@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:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_head { this: np:hasAssertion dgn-np:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_assertion; np:hasProvenance dgn-np:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_provenance; np:hasPublicationInfo dgn-np:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_publicationInfo; a np:Nanopublication . dgn-np:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_assertion a np:Assertion . dgn-np:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_provenance a np:Provenance . dgn-np:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_publicationInfo a np:PublicationInfo . } dgn-np:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_assertion { miriam-gene:7161 a ncit:C16612 . lld:C1762616 a ncit:C7057 . dgn-gda:DGN4d4e338eae91a3fc7ab75e44ab5b8362 sio:SIO_000628 miriam-gene:7161, lld:C1762616; a sio:SIO_001121 . } dgn-np:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_provenance { dgn-np:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_assertion dcterms:description "[Based on the hypothesis that meningiomas cumulatively acquire genetic alterations and thus progress from the benign to the atypical and anaplastic states, genetic alterations in the methylation status of p73 or RASSF1A along with 1p LOH may result in the malignant transformation of a meningioma.]. 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:17695396; 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:NP755751.RA1qd6Qpwz7LOpWZ-bUMuG27c98FlZOVDe55Yuqh5LGHg130_publicationInfo { this: dcterms:created "2015-08-25T14:45:16+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" . }