@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:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_head { this: np:hasAssertion dgn-np:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_assertion; np:hasProvenance dgn-np:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_provenance; np:hasPublicationInfo dgn-np:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_publicationInfo; a np:Nanopublication . dgn-np:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_assertion a np:Assertion . dgn-np:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_provenance a np:Provenance . dgn-np:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_publicationInfo a np:PublicationInfo . } dgn-np:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_assertion { miriam-gene:5925 a ncit:C16612 . lld:C0585442 a ncit:C7057 . dgn-gda:DGN8a6acf6b89f4be63cfe2025a163dff44 sio:SIO_000628 miriam-gene:5925, lld:C0585442; a sio:SIO_001123 . } dgn-np:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_provenance { dgn-np:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_assertion dcterms:description "[The frequencies of each type of abnormalities were: structural anomalies, 28.6% (18 of 63); subtle mutations, 6.0% (3 of 50); negative protein expression, 53.6% (30 of 56); 54.5% (18 of 33) of tumors with LOH at the Rb locus were proved to show negative Rb expression, while 50.0% (11 of 22) of tumors without LOH also showed negative Rb, indicating that LOH at the Rb locus in osteosarcoma will not necessarily correlate with the actual inactivation of the Rb gene at the protein level.]. 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:8187094; 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:NP1335061.RAvsVCGwc_0B3zUVNrDfBlhZjyXpDL8Hka4QfaDElJxUo130_publicationInfo { this: dcterms:created "2016-05-13T12:51:51+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" . }