@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:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_head { this: np:hasAssertion dgn-np:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_assertion; np:hasProvenance dgn-np:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_provenance; np:hasPublicationInfo dgn-np:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_publicationInfo; a np:Nanopublication . dgn-np:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_assertion a np:Assertion . dgn-np:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_provenance a np:Provenance . dgn-np:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_publicationInfo a np:PublicationInfo . } dgn-np:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C1168401 a ncit:C7057 . dgn-gda:DGN020fbfdf14bc9db6af323e788b03e529 sio:SIO_000628 miriam-gene:7157, lld:C1168401; a sio:SIO_001121 . } dgn-np:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_provenance { dgn-np:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_assertion dcterms:description "[We performed a molecular analysis of the frequency and spectrum of p53 gene mutations in 40 cell lines (23 from oral cavity tumours and 17 from larynx tumours) derived from 33 patients with squamous cell carcinoma of the head and neck (SCCHN).]. 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:9288320; 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:NP1380048.RALIUAbcJVkazb1hwwS7OEHWWIclwig_Pj8G3Y3qRtVuQ130_publicationInfo { this: dcterms:created "2016-05-13T12:52:11+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" . }