@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:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_head { this: np:hasAssertion dgn-np:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_assertion; np:hasProvenance dgn-np:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_provenance; np:hasPublicationInfo dgn-np:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_publicationInfo; a np:Nanopublication . dgn-np:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_assertion a np:Assertion . dgn-np:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_provenance a np:Provenance . dgn-np:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_publicationInfo a np:PublicationInfo . } dgn-np:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0085390 a ncit:C7057 . dgn-gda:DGN642e19011d06d09bf756273144b1cc01 sio:SIO_000628 miriam-gene:7157, lld:C0085390; a sio:SIO_001121 . } dgn-np:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_provenance { dgn-np:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_assertion dcterms:description "[The database describes each p53 mutation (type of the mutation, exon and codon affected by the mutation, nucleotide and amino acid change), each family (family history of cancer, diagnosis of Li-Fraumeni syndrome), each affected individual (sex, generation, p53 status, from which parent the mutation was inherited) and each tumour (type, age of onset, p53 status-loss of heterozygosity, immunostaining).]. 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:9399838; 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:NP1385401.RA4xL9-JyDF4wHqX-LgP9FuDrVBsSVN1FkMNLU3raLFMA130_publicationInfo { this: dcterms:created "2016-05-13T12:52:14+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" . }