@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:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_head { this: np:hasAssertion dgn-np:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_assertion; np:hasProvenance dgn-np:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_provenance; np:hasPublicationInfo dgn-np:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_publicationInfo; a np:Nanopublication . dgn-np:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_assertion a np:Assertion . dgn-np:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_provenance a np:Provenance . dgn-np:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0007137 a ncit:C7057 . dgn-gda:DGN1ada1bbfc4c5ac56a270d62be80040c7 sio:SIO_000628 miriam-gene:7157, lld:C0007137; a sio:SIO_001121 . } dgn-np:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_provenance { dgn-np:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_assertion dcterms:description "[The only correlation between these genetic alterations and clinicopathologic characteristics was that mutations of the p53 gene were detected more frequently in oral SCCs with lymph node metastasis than in those without it (P < 0.05).]. 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:8887073; 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:NP1361001.RAGg0L9uUp9Nn7KyfUcojoKefgdDLZEJE3Gsip3Pd4LFY130_publicationInfo { this: dcterms:created "2016-05-13T12:52:03+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" . }