Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance.
- NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_assertion description "[Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance.
- NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_assertion evidence source_evidence_literature NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance.
- NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_assertion SIO_000772 11527935 NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance.
- NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_assertion wasDerivedFrom befree-2016 NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance.
- NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_assertion wasGeneratedBy ECO_0000203 NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP328631.RAtGbKzBfdao2l5VdLShmat20E2kiP6JwKWfk3GzWFn8Y130_provenance.