@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_head { this: np:hasAssertion dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_assertion; np:hasProvenance dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_provenance; np:hasPublicationInfo dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_publicationInfo; a np:Nanopublication . dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_assertion a np:Assertion . dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_provenance a np:Provenance . dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_publicationInfo a np:PublicationInfo . } dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_assertion { miriam-gene:2064 a ncit:C16612 . lld:C0005684 a ncit:C7057 . dgn-gda:DGNb3e1ce261fc8b547e6f3674df5b2af52 sio:SIO_000628 miriam-gene:2064, lld:C0005684; a sio:SIO_001122 . } dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_provenance { dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_assertion dcterms:description "[These data suggest that this SNP has variable frequency in different ethnic groups. In addition, intraracial differences in allele frequency were seen. The presence of the Val allele in the African-American population, but not in the African population is]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:11106692; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP68546.RAefH1xGdRnmqOsIwwmopZ6BaN7aRDwk1oPeD64bKQ4IY130_publicationInfo { this: dcterms:created "2016-05-13T12:42:19+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }