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- source_evidence_literature type ECO_0000212 NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_provenance.
- NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_assertion description "[Recessive mutant alleles of MYO7A, USH1C, CDH23, and PCDH15 cause non-syndromic deafness or type 1 Usher syndrome (USH1) characterised by deafness, vestibular areflexia, and vision loss due to retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_provenance.
- NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_assertion evidence source_evidence_literature NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_provenance.
- NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_assertion SIO_000772 21940737 NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_provenance.
- NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_assertion wasDerivedFrom befree-20150227 NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_provenance.
- NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_assertion wasGeneratedBy ECO_0000203 NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584098.RA85cNFea1or47a1oVOoY4b0g_76ReVwzIkyzuxgCbpBA130_provenance.