Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance.
- NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_assertion description "[We have made use of individuals with overlapping deletions producing choroideremia as part of a complex phenotype, to define the boundaries on the X chromosome for this gene, as well as for X-linked mixed deafness with perilymphatic gusher (DFN3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance.
- NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_assertion evidence source_evidence_literature NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance.
- NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_assertion SIO_000772 2491012 NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance.
- NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_assertion wasDerivedFrom befree-20150227 NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance.
- NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_assertion wasGeneratedBy ECO_0000203 NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_provenance.