Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_assertion> ?p ?o ?g. }
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- NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_assertion type Assertion NP22543.RA09hLn3MutXPv-pEdZTKB32z2iX19JCRRtokHd7STz8Q130_head.
- 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.