Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_assertion type Assertion NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_head.
- NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_assertion description "[Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_provenance.
- NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_assertion evidence source_evidence_literature NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_provenance.
- NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_assertion SIO_000772 23559863 NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_provenance.
- NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_assertion wasDerivedFrom befree-20150227 NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_provenance.
- NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_assertion wasGeneratedBy ECO_0000203 NP584167.RAscy5_Ig2ZtbiXeWIUxwiDNQTzvEwwZBN-IrlGGFhWU8130_provenance.