Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance.
- NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_assertion description "[Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance.
- NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_assertion evidence source_evidence_curated NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance.
- NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_assertion SIO_000772 10533068 NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance.
- NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_assertion wasDerivedFrom uniprot-20130724 NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance.
- NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_assertion wasGeneratedBy ECO_0000218 NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP5637.RAruv_IoN3Fvdsxz6jqWxqHEH6cNNa_a6ZK1dkixn848g130_provenance.