Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.
- NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.
- NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_assertion evidence source_evidence_literature NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.
- NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_assertion SIO_000772 10644430 NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.
- NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_assertion wasDerivedFrom befree-20150227 NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.
- NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_assertion wasGeneratedBy ECO_0000203 NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP635692.RAHGHF-X4789WVvS55cnrXccoS203Hcv0VSR2ieaUEUVA130_provenance.