@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:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_head { this: np:hasAssertion dgn-np:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_assertion; np:hasProvenance dgn-np:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_provenance; np:hasPublicationInfo dgn-np:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_publicationInfo; a np:Nanopublication . dgn-np:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_assertion a np:Assertion . dgn-np:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_provenance a np:Provenance . dgn-np:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_publicationInfo a np:PublicationInfo . } dgn-np:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_assertion { miriam-gene:79139 a ncit:C16612 . lld:C0008626 a ncit:C7057 . dgn-gda:DGN559dae063660f52f03cc87b01046aad3 sio:SIO_000628 miriam-gene:79139, lld:C0008626; a sio:SIO_001121 . } dgn-np:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_provenance { dgn-np:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_assertion dcterms:description "[The results indicated that M-FISH exhibited obvious chromosomal aberrations with high frequency including translocation, insertion, breakage and rearrangement, deletion and increasement of chromosome number, the complex karyotype of MUTZ-1 was shown as 50, xx, der (1) t (1;2), ins (1;14), +der (2) t(2;19), der (3) t (3;5), der (3) (3::5::22), 5q-, der (6) t (3;6), der (7) (18::7::17), +8, +der (9) t (1;9), der (10) t (1;10), +11, +12, der (?13) (10::13::5::8), der (14) t (8;14), der (14) t (14, 15), der (15) t (15;21) x 2, +17, +18, -21, -22.]. 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:16584590; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP942563.RApPs6NHOGEfPKxGyTYRHEa29UKWyMoppkCkpicCKVdlc130_publicationInfo { this: dcterms:created "2015-08-25T14:47:15+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }