Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.
- NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_assertion description "[Earlier, the peripherin/RDS Arg-172-Trp mutation was associated primarily with a macular degeneration phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.
- NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_assertion evidence source_evidence_literature NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.
- NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_assertion SIO_000772 9810570 NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.
- NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_assertion wasDerivedFrom befree-2016 NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.
- NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_assertion wasGeneratedBy ECO_0000203 NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1407862.RAD-qrA00uDZq8HrF3Cn9eAjvNDFS4557Mh35md17wMbk130_provenance.