Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_assertion> ?p ?o ?g. }
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- NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_assertion type Assertion NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_head.
- NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_assertion description "[A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_provenance.
- NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_assertion evidence source_evidence_literature NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_provenance.
- NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_assertion SIO_000772 25477324 NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_provenance.
- NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_assertion wasDerivedFrom befree-2016 NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_provenance.
- NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_assertion wasGeneratedBy ECO_0000203 NP1245073.RAKNRVysEoHHaCXXeDwDUPPVjbbKod6Am5lY3BSoaO-oE130_provenance.