http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#head
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#assertion
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#provenance
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#assertion
http://rdf.disgenet.org/resource/gda/DGNa0a262d12ec63fe95422ce0fe1f3c2d7
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/2969
http://rdf.disgenet.org/resource/gda/DGNa0a262d12ec63fe95422ce0fe1f3c2d7
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0009241
http://rdf.disgenet.org/resource/gda/DGNa0a262d12ec63fe95422ce0fe1f3c2d7
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001121
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#provenance
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#assertion
http://purl.org/dc/terms/description
[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/22608712
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/dc/terms/created
2017-10-17T13:13:11+02:00
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP472265.RAml95ufb2DBOSKk_DOjogViaD-_JDKjx4wFWtI5QM0jc
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0