http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#head
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#assertion
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#provenance
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#assertion
http://rdf.disgenet.org/resource/gda/DGNd64e1c9e492a4a3db0f3ae3c58d24cac
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/4671
http://rdf.disgenet.org/resource/gda/DGNd64e1c9e492a4a3db0f3ae3c58d24cac
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0026847
http://rdf.disgenet.org/resource/gda/DGNd64e1c9e492a4a3db0f3ae3c58d24cac
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#provenance
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#assertion
http://purl.org/dc/terms/description
[Our results suggest that extent of deletions encompassing H4F5, SMN1, NAIP and copy number of SMN2 gene can modify the SMA phenotype, thus accounting for the different clinical subtypes of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#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/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/16000867
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#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/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/dc/terms/created
2017-10-17T13:14:55+02:00
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP742900.RASjmrfh4rsLYo-h-FAlvCFinlrcnKVE4ZJdNZxms6Bso
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