Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance.
- NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_assertion wasGeneratedBy ECO_0000203 NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance.
- NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_assertion wasDerivedFrom befree-20140225 NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance.
- NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_assertion SIO_000772 21616938 NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance.
- NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_assertion evidence source_evidence_literature NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance.
- NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_assertion description "[A homozygous mutation in the RAD51C gene was recently found to cause Fanconi anemia-like disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP564676.RAJw9c-TlXCoaNJG1ilM7r063CZLJ6d55bKUKkUfARBLk130_provenance.