@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:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_head { this: np:hasAssertion dgn-np:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_assertion; np:hasProvenance dgn-np:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_provenance; np:hasPublicationInfo dgn-np:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_publicationInfo; a np:Nanopublication . dgn-np:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_assertion a np:Assertion . dgn-np:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_provenance a np:Provenance . dgn-np:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_publicationInfo a np:PublicationInfo . } dgn-np:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_assertion { miriam-gene:1029 a ncit:C16612 . lld:C0025202 a ncit:C7057 . dgn-gda:DGN0d22676dd76941f68bfdacd9d76871c5 sio:SIO_000628 miriam-gene:1029, lld:C0025202; a sio:SIO_001121 . } dgn-np:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_provenance { dgn-np:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_assertion dcterms:description "[A number of genes previously recognized to have an important role in the development and progression of melanoma were identified including homozygous deletions of CDKN2A (13 of 39 samples), CDKN2B (10 of 39), PTEN (3 of 39), PTPRD (3 of 39), TP53 (1 of 39), and amplifications of CCND1 (2 of 39), MITF (2 of 39), MDM2 (1 of 39), and NRAS (1 of 39).]. 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:22250051; 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:NP953782.RAn0ZvX1h4fDrsYjhAVIp86CHdVoQCewMHqSBjHNQ6mlI130_publicationInfo { this: dcterms:created "2016-05-13T12:48:57+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" . }