Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance.
- NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_assertion description "[In addition, we report three new pseudodominant families that now comprise eight of 178 outbred STGD1 families and suggest a carrier frequency of STGD1-associated ABCR mutations of about 4.5% (approximately 1/22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance.
- NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_assertion evidence source_evidence_curated NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance.
- NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_assertion SIO_000772 11379881 NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance.
- NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_assertion wasDerivedFrom uniprot-2016 NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance.
- NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_assertion wasGeneratedBy ECO_0000218 NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1430.RAKIX6eT18vxicMG5UQeP5SRNPLSiTt5w0-8Rk8VEYUZs130_provenance.