@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:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_head { this: np:hasAssertion dgn-np:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_assertion; np:hasProvenance dgn-np:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_provenance; np:hasPublicationInfo dgn-np:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_publicationInfo; a np:Nanopublication . dgn-np:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_assertion a np:Assertion . dgn-np:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_provenance a np:Provenance . dgn-np:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_publicationInfo a np:PublicationInfo . } dgn-np:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0278996 a ncit:C7057 . dgn-gda:DGNb87b448fdd003aebe21965960d743705 sio:SIO_000628 miriam-gene:7157, lld:C0278996; a sio:SIO_001121 . } dgn-np:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_provenance { dgn-np:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_assertion dcterms:description "[Application of these findings to clinical problems include the identification of p53 mutations as markers for malignant change in Barrett's epithelium, the use of discordant p53 mutations to diagnose second primary malignant neoplasms in patients with head and neck cancer, and the potential for therapy by the reversal of genetic lesions.]. 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:1444790; 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:NP413657.RAufolDIysC2i7hewJhRag6ga7_MCtYXdCDWHCX94Hl6M130_publicationInfo { this: dcterms:created "2016-05-13T12:44:52+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" . }