Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance.
- NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_assertion wasGeneratedBy ECO_0000203 NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance.
- NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_assertion wasDerivedFrom befree-20150227 NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance.
- NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_assertion SIO_000772 23852183 NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance.
- NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_assertion evidence source_evidence_literature NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance.
- NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_assertion description "[VWD is classified into quantitative deficiencies of VWF (type 1 and type 3 VWD) and qualitative variants (type 2 VWD), because of a dysfunctional VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776315.RABSVzLYVKjog8YQq_U_hUa6bazU2tEEYKvLFMf5xJpHo130_provenance.