Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_assertion> ?p ?o ?g. }
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- NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_assertion type Assertion NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_head.
- NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_assertion description "[The retinal dystrophy associated with the Pro23Ala mutation is characteristically mild in presentation and course, with greater preservation of ERG amplitudes than the more prevalent Pro23His mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_provenance.
- NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_assertion evidence source_evidence_literature NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_provenance.
- NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_assertion SIO_000772 10980774 NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_provenance.
- NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_assertion wasDerivedFrom befree-20150227 NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_provenance.
- NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_assertion wasGeneratedBy ECO_0000203 NP383267.RA44rA2yszy36KHRnqv4LGCnuM2n4U1bFn4xEjvgwH0YE130_provenance.