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- NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_assertion type Assertion NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_head.
- NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_assertion wasGeneratedBy ECO_0000203 NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_provenance.
- NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_assertion wasDerivedFrom befree-20140225 NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_provenance.
- NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_assertion SIO_000772 22004887 NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_provenance.
- NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_assertion evidence source_evidence_literature NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_provenance.
- NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_assertion description "[This report provide a wide spectrum of USH2A mutations and clinical features, including atypical Usher syndrome phenotypes resembling Usher syndrome type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812692.RAAS-d95m4hpYj1Ae7W2Xevhxap1bHUnGQicAHJ3gcqE8130_provenance.