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- source_evidence_literature type ECO_0000212 NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_provenance.
- NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_assertion description "[Intrafamilial phenotypic variability in families with RDS mutations: exclusion of ROM1 as a genetic modifier for those with retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_provenance.
- NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_assertion evidence source_evidence_literature NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_provenance.
- NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_assertion SIO_000772 16916875 NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_provenance.
- NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_assertion wasDerivedFrom befree-2016 NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_provenance.
- NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_assertion wasGeneratedBy ECO_0000203 NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_provenance.
- befree-2016 importedOn "2016-02-19" NP564819.RA7o0G1b0yi4-So3qfVEew3qyG1xR22jQNjeUgRib7dRU130_provenance.