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- source_evidence_literature type ECO_0000212 NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the 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.
- NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_assertion evidence source_evidence_literature NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_provenance.
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- befree-20150227 importedOn "2015-02-27" NP954505.RA7gg-oS-BwlXWmUdxpyyydW3-jCapVEjytuI1vuQZ7B4130_provenance.