Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance.
- NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_assertion wasGeneratedBy ECO_0000203 NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance.
- NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_assertion wasDerivedFrom befree-20140225 NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance.
- NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_assertion SIO_000772 23446638 NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance.
- NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_assertion evidence source_evidence_literature NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance.
- NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_assertion description "[KLLN variants in CS/CSL patients are rare (1 of 136, 0.007%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP644221.RA9LqY3YAxnZWIf16GGc0omnBobcygmNBXsEaghsAPdz8130_provenance.