@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:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_head { this: np:hasAssertion dgn-np:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_assertion; np:hasProvenance dgn-np:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_provenance; np:hasPublicationInfo dgn-np:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_publicationInfo; a np:Nanopublication . dgn-np:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_assertion a np:Assertion . dgn-np:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_provenance a np:Provenance . dgn-np:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_publicationInfo a np:PublicationInfo . } dgn-np:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_assertion { miriam-gene:4292 a ncit:C16612 . lld:C1321489 a ncit:C7057 . dgn-gda:DGN3e4ff48a29ac41e874aa18da1033c422 sio:SIO_000628 miriam-gene:4292, lld:C1321489; a sio:SIO_001121 . } dgn-np:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_provenance { dgn-np:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_assertion dcterms:description "[To determine if the tumours of patients with MTS have widespread genomic instability and whether loss of heterozygosity (LOH) in the chromosomal regions containing hMSH2 and hMLH1 is detectable, MSI and LOH were examined at 10 dinucleotide repeats on chromosomes 2p, 3p, 5q, 9p, 17p and 18q.]. 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:9349329; 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:NP1382830.RAY0Mk6y8jO3laV1NPod7rYvjhuNY_lo4_OI11viu_Ao0130_publicationInfo { this: dcterms:created "2016-05-13T12:52:13+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" . }