Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion> ?p ?o ?g. }
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- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion type Assertion NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_head.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion wasGeneratedBy ECO_0000203 NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion wasDerivedFrom befree-20140225 NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion SIO_000772 22004887 NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_assertion evidence source_evidence_literature NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.
- NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_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." NP476152.RAeew8lSIL9dJMi03pKfI2wBB_NT50VDYuxnSLfioia-Q130_provenance.