@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:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_head { this: np:hasAssertion dgn-np:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_assertion; np:hasProvenance dgn-np:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_provenance; np:hasPublicationInfo dgn-np:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_publicationInfo; a np:Nanopublication . dgn-np:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_assertion a np:Assertion . dgn-np:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_provenance a np:Provenance . dgn-np:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_publicationInfo a np:PublicationInfo . } dgn-np:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_assertion { miriam-gene:100528024 a ncit:C16612 . lld:C0025362 a ncit:C7057 . dgn-gda:DGNc46db3958a82a9c21d841574964eae1a sio:SIO_000628 miriam-gene:100528024, lld:C0025362; a sio:SIO_001121 . } dgn-np:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_provenance { dgn-np:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_assertion dcterms:description "[The remaining four had chromosomal rearrangements: an unbalanced translocation, t(11;13), with a deletion including the WAGR (Wilms' tumor, aniridia, genitourinary abnormalities, and mental retardation) region, and three balanced rearrangements with what appear to be position effect breakpoints 3' of PAX6: (a) a t(7;11) with the 11p13 breakpoint approximately 30 kb downstream of PAX6, (b) a dir ins(12;11) with a breakpoint >50 kb from PAX6, and (c) an inv(11)(p13q13) with a breakpoint >75 kb downstream of PAX6.]. 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:12386836; 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:NP1015418.RAQsFmifgTgrC91T5cBu-NwoAoXH7q0II7pyd7wvbZE5Q130_publicationInfo { this: dcterms:created "2015-08-25T14:48:10+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" . }