Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.
- NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_assertion wasGeneratedBy ECO_0000203 NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.
- NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_assertion wasDerivedFrom befree-20150227 NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.
- NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_assertion SIO_000772 8045710 NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.
- NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_assertion evidence source_evidence_literature NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.
- NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668542.RAUPpCZQ5uK_kVe1YZ7S6kj88QjItPDk5h9LWU1ZxlVUc130_provenance.