Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance.
- NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_assertion description "[Deficiency of C1INH results in hereditary angioedema, a disease characterised by episodes of angioedema of the skin or the mucosa of the gastrointestinal tract or the oropharynx.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance.
- NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_assertion evidence source_evidence_literature NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance.
- NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_assertion SIO_000772 20806108 NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance.
- NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_assertion wasDerivedFrom befree-2016 NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance.
- NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_assertion wasGeneratedBy ECO_0000203 NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance.
- befree-2016 importedOn "2016-02-19" NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_provenance.