@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:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_head { this: np:hasAssertion dgn-np:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_assertion; np:hasProvenance dgn-np:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_provenance; np:hasPublicationInfo dgn-np:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_publicationInfo; a np:Nanopublication . dgn-np:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_assertion a np:Assertion . dgn-np:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_provenance a np:Provenance . dgn-np:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_publicationInfo a np:PublicationInfo . } dgn-np:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_assertion { miriam-gene:1019 a ncit:C16612 . lld:C0007114 a ncit:C7057 . dgn-gda:DGN89ab61ab01f7afe6964fbbd54f2d928d sio:SIO_000628 miriam-gene:1019, lld:C0007114; a sio:SIO_001121 . } dgn-np:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_provenance { dgn-np:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_assertion dcterms:description "[We examined the frequency of INK4a-ARF, p53, and CDK4 mutations in skin carcinomas from patients with xeroderma pigmentosum (XP), a rare autosomal disease that is associated with a defect in DNA repair and that predisposes patients to skin cancer.]. 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:11078762; 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:NP300466.RAAZsAgADdHKcuneOTs10dc9a_0ij4-5hM9ODEHY1PHA8130_publicationInfo { this: dcterms:created "2016-05-13T12:44:02+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" . }