Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP202122.RAaTT-k_c1iOrX468wp28HtEN7afNjr2dUsuRI4tn5j64130_provenance.