Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_assertion> ?p ?o ?g. }
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- NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_assertion type Assertion NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_head.
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- NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_assertion wasDerivedFrom befree-20150227 NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_provenance.
- NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_assertion SIO_000772 14740321 NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_provenance.
- NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_assertion evidence source_evidence_literature NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_provenance.
- NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_assertion description "[The identification of additional VLGR1 mutations to test whether a phenotype/genotype correlation exists, akin to that shown for other Usher syndrome disease genes, is warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_provenance.