Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_assertion> ?p ?o ?g. }
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- NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_assertion type Assertion NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_head.
- NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_assertion description "[Five non-syndromic deaf individuals were identified with normal retinal and vestibular phenotypes that segregate compound heterozygous mutations of CDH23, where one mutation is a known or predicted USH1 allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_provenance.
- NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_assertion evidence source_evidence_literature NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_provenance.
- NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_assertion SIO_000772 21940737 NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_provenance.
- NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_assertion wasDerivedFrom befree-2016 NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_provenance.
- NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_assertion wasGeneratedBy ECO_0000203 NP925809.RAtfbLR2LNCxcpFONRRf-w9RJxInSpYrs3sW0R3CiI_KY130_provenance.