Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance.
- NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_assertion description "[To examine the role of RP1 mutations in RP, we screened 101 unrelated Chinese RP patients (unselected for mode of inheritance) and 190 elderly normal control subjects for sequence changes in the coding exons for the 2156 amino acid RP1 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance.
- NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_assertion evidence source_evidence_literature NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance.
- NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_assertion SIO_000772 11317367 NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance.
- NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_assertion wasDerivedFrom befree-20150227 NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance.
- NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_assertion wasGeneratedBy ECO_0000203 NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674430.RAgyhHeTbfpaGUxUXPNRzojO8A_1qSWFS1fFiZdRF74ZE130_provenance.