Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion> ?p ?o ?g. }
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- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion type Assertion NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_head.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion evidence source_evidence_literature NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion SIO_000772 1610568 NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion wasDerivedFrom befree-20140225 NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.
- NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_assertion wasGeneratedBy ECO_0000203 NP492714.RA6__-yTxGsUd1h0O3au7M0_UoLMoz-RPM6L5Krlk1HF0130_provenance.