@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:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_head { this: np:hasAssertion dgn-np:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_assertion; np:hasProvenance dgn-np:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_provenance; np:hasPublicationInfo dgn-np:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_publicationInfo; a np:Nanopublication . dgn-np:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_assertion a np:Assertion . dgn-np:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_provenance a np:Provenance . dgn-np:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_publicationInfo a np:PublicationInfo . } dgn-np:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0017638 a ncit:C7057 . dgn-gda:DGNd35a06948e61122b53b49a6ba5b93258 sio:SIO_000628 miriam-gene:7157, lld:C0017638; a sio:SIO_001121 . } dgn-np:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_provenance { dgn-np:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_assertion dcterms:description "[Using the methods of restriction fragment length polymorphism (RFLP) and single strand conformation polymorphism (SSCP) analyses, we have examined 33 cases of human gliomas with various malignant grades to detect the deletions of putative tumor suppressor gene loci, chromosome 10, 13q(retinoblastoma gene, Rb), 17p, and 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:8924230; 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:NP1362775.RAwcHl6J8ixAf7siyEq0hK2-pS8KAmyYAluTVZ92zy0A8130_publicationInfo { this: dcterms:created "2016-05-13T12:52:03+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" . }