@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:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_head { this: np:hasAssertion dgn-np:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_assertion; np:hasProvenance dgn-np:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_provenance; np:hasPublicationInfo dgn-np:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_publicationInfo; a np:Nanopublication . dgn-np:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_assertion a np:Assertion . dgn-np:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_provenance a np:Provenance . dgn-np:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_publicationInfo a np:PublicationInfo . } dgn-np:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0004114 a ncit:C7057 . dgn-gda:DGN714c45c4ed2a654f055d8003182fe9ab sio:SIO_000628 miriam-gene:7157, lld:C0004114; a sio:SIO_001121 . } dgn-np:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_provenance { dgn-np:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_assertion dcterms:description "[These findings suggest that histologically indistinguishable, low-grade astrocytic gliomas that are destined to progress to higher grades, do so along two distinct clinicopathologic pathways (either stepwise to anaplastic glioma, then glioblastoma, or directly to glioblastoma) marked by the presence or absence of p53 mutation.]. 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:8007011; 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:NP1329721.RAnQe8PqZbKkWuUv4l5xYOWkbx0WZguBjS-vAj8uZMUKg130_publicationInfo { this: dcterms:created "2016-05-13T12:51:49+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" . }