Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance.
- NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_assertion description "[This article provides evidence of the wide clinical spectrum of cancer susceptibility associated with a BAP1 germline mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance.
- NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_assertion evidence source_evidence_literature NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance.
- NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_assertion SIO_000772 23585512 NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance.
- NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_assertion wasDerivedFrom befree-20150227 NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance.
- NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_assertion wasGeneratedBy ECO_0000203 NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP794442.RA9o4ayxKAGvJ3Mi-G9lyrHTuRV_aaCtYLP_STI8dcYi0130_provenance.