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<http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec> <http://www.nanopub.org/nschema#hasPublicationInfo> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_publicationInfo> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_head> .
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<http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Assertion> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_head> .
<http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Provenance> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_head> .
<http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_publicationInfo> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#PublicationInfo> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_head> .
<http://identifiers.org/ncbigene/26191> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0011860> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNf91a90bc224bbae4b742b8927be95325> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/26191> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNf91a90bc224bbae4b742b8927be95325> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0011860> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNf91a90bc224bbae4b742b8927be95325> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001122> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> <http://purl.org/dc/terms/description> "[To evaluate the impact of a functional variation in the PTPN22 gene in type 1 (T1D) and type 2 diabetes (T2D), the PTPN22 C1858T single nucleotide polymorphism (SNP) was studied in the population of Estonian origin, including 170 T1D patients, 244 T2D patients and 230 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> <http://purl.org/ontology/wi/core#evidence> <http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> <http://semanticscience.org/resource/SIO_000772> <http://identifiers.org/pubmed/18764813> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> <http://www.w3.org/ns/prov#wasDerivedFrom> <http://rdf.disgenet.org/v2.1.0/void.ttl#gad-20130706> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_assertion> <http://www.w3.org/ns/prov#wasGeneratedBy> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000203> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#gad-20130706> <http://purl.org/pav/2.0/importedOn> "2013-07-06"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000212> <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#comment> "Gene-disease associations inferred from text-mining the literature."@en <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#label> "DisGeNET evidence - LITERATURE"@en <http://rdf.disgenet.org/nanopublications.trig#NP67735.RA98q3E5A5fQt2QpNMb-Xv8ULi4IL5QcrcnOIXQP_epec130_provenance> .
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