Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance.
- NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_assertion description "[Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance.
- NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_assertion evidence source_evidence_curated NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance.
- NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_assertion SIO_000772 10802646 NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance.
- NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_assertion wasDerivedFrom ctd_human-20130708 NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance.
- NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_assertion wasGeneratedBy ECO_0000218 NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_provenance.