Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance.
- NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_assertion description "[Using the Universal Mutation Database (UMD) software, we have constructed UMD-USHbases, a set of relational databases of nucleotide variations for seven genes involved in Usher syndrome (MYO7A, CDH23, PCDH15, USH1C, USH1G, USH3A and USH2A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance.
- NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_assertion evidence source_evidence_literature NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance.
- NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_assertion SIO_000772 18484607 NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance.
- NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_assertion wasDerivedFrom befree-2016 NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance.
- NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_assertion wasGeneratedBy ECO_0000203 NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP671479.RAZLa0iS52gwVbTbXlaoZpY8xII0yvEMzrWlUZn__zA3Y130_provenance.