Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_assertion> ?p ?o ?g. }
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- NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_assertion type Assertion NP836048.RA2EVuiHu54Kz0WWP_HFu9HHojQHyYpFi_YdAIALBoYKw130_head.
- 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.