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- source_evidence_literature type ECO_0000212 NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.
- NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_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." NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.
- NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_assertion evidence source_evidence_literature NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.
- NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_assertion SIO_000772 1610568 NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.
- NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_assertion wasDerivedFrom befree-20150227 NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.
- NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_assertion wasGeneratedBy ECO_0000203 NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674084.RA80OtWhh5TToEtOYCrhjOtW8WRC-8ldKLOp0YSZqgDqI130_provenance.