Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance.
- NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_assertion description "[Collectively, these data identify a primary disease-causing molecular defect in cone cells and suggest that RDS-associated disease in patients may be a result of this defect coupled with secondary sequellae involving RPE and choriocapillaris cell loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance.
- NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_assertion evidence source_evidence_literature NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance.
- NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_assertion SIO_000772 24463884 NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance.
- NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_assertion wasDerivedFrom befree-20150227 NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance.
- NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_assertion wasGeneratedBy ECO_0000203 NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP668573.RAcRNS9uKultPut4UWEovtMouvPmNFGjNVuB3vMhF0dSU130_provenance.