@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:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_head { this: np:hasAssertion dgn-np:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_assertion; np:hasProvenance dgn-np:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_provenance; np:hasPublicationInfo dgn-np:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_publicationInfo; a np:Nanopublication . dgn-np:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_assertion a np:Assertion . dgn-np:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_provenance a np:Provenance . dgn-np:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_assertion { miriam-gene:4255 a ncit:C16612 . lld:C0027627 a ncit:C7057 . dgn-gda:DGN675004086ca5204462030dd5d479dbdc sio:SIO_000628 miriam-gene:4255, lld:C0027627; a sio:SIO_001121 . } dgn-np:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_provenance { dgn-np:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_assertion dcterms:description "[Detection of certain molecular markers such as deletion of 1p and 19q chromosomal arms, hypermethylation of MGMT promoter, and characteristic PTEN exon mutations may help differentiate subtypes which are more prone to extracranial metastases.]. 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:24447608; 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:NP1147026.RAbPcCbK6Iu9t2HRvwADuP0XDtHMLqbMg3tX6Ed__X8uY130_publicationInfo { this: dcterms:created "2016-05-13T12:50:26+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" . }