@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:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_head { this: np:hasAssertion dgn-np:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_assertion; np:hasProvenance dgn-np:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_provenance; np:hasPublicationInfo dgn-np:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_publicationInfo; a np:Nanopublication . dgn-np:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_assertion a np:Assertion . dgn-np:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_provenance a np:Provenance . dgn-np:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_publicationInfo a np:PublicationInfo . } dgn-np:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C1134719 a ncit:C7057 . dgn-gda:DGN8193154571cf96e713786e1b35501fec sio:SIO_000628 miriam-gene:7157, lld:C1134719; a sio:SIO_001122 . } dgn-np:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_provenance { dgn-np:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_assertion dcterms:description "[P53 mutations were evident in five breast cancer patients (17%) including two missense mutations (A218 T and R279 G) in exon 6, 8; nonsense mutations (S297stop and Y159stop) in exon 8, 5, respectively, and frame shift mutation (M133 fs) in exon 5. p53 mutations were associated with invasive ductal carcinoma, large tumor size, and advanced disease stage]. 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:20015931; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP753992.RAmUj8Lc6buNmPiBa096MWq79uI1BqIbmc--FkTogZG14130_publicationInfo { this: dcterms:created "2015-08-25T14:45:15+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }