Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance.
- NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_assertion wasGeneratedBy ECO_0000203 NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance.
- NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_assertion wasDerivedFrom befree-20150227 NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance.
- NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_assertion SIO_000772 16757530 NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance.
- NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_assertion evidence source_evidence_literature NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance.
- NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_assertion description "[In addition to the HLRCC case with the N64T germline FH mutation, we identified one other LCT with a previously unreported FH mutation (M411I).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533039.RABHkaW4j5xJVfhwAY1FOiI34NWFZ2mmPZkcIhtYoEhR4130_provenance.