@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:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_head { this: np:hasAssertion dgn-np:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_assertion; np:hasProvenance dgn-np:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_provenance; np:hasPublicationInfo dgn-np:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_publicationInfo; a np:Nanopublication . dgn-np:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_assertion a np:Assertion . dgn-np:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_provenance a np:Provenance . dgn-np:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_publicationInfo a np:PublicationInfo . } dgn-np:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_assertion { miriam-gene:1029 a ncit:C16612 . lld:C0025202 a ncit:C7057 . dgn-gda:DGNcdae8ad451c72e5897785820425fb543 sio:SIO_000628 miriam-gene:1029, lld:C0025202; a sio:SIO_001121 . } dgn-np:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_provenance { dgn-np:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_assertion dcterms:description "[The objectives of this study were to determine the frequency of family history of melanoma in MPM cases, to characterize other clinical features including history of other cancer, and to determine the association with functional CDKN2A mutations.]. 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:12001124; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP354323.RAnvodtqtWOoRTuU-eiLi0QRwtLWQPUQVIOtlp-7H3UZE130_publicationInfo { this: dcterms:created "2016-05-13T12:44:26+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" . }