Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_assertion> ?p ?o ?g. }
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- NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_assertion type Assertion NP635694.RASzhHrYbtrnlbxRUKDOZQr1ZFRtsqGfxvW11k-tnZbg4130_head.
- 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.