Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_assertion> ?p ?o ?g. }
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- NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_assertion type Assertion NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_head.
- NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_assertion description "[The 208delG mutation in the FSCN2 gene produces not only autosomal dominant retinitis pigmentosa but also ADMD (autosomal dominant macular degeneration) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance.
- NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_assertion evidence source_evidence_literature NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance.
- NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_assertion SIO_000772 14609921 NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance.
- NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_assertion wasDerivedFrom lhgdn-20090331 NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance.
- NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_assertion wasGeneratedBy ECO_0000203 NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance.