Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_assertion> ?p ?o ?g. }
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- NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_assertion type Assertion NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_head.
- NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_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." NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_provenance.
- NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_assertion evidence source_evidence_literature NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_provenance.
- NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_assertion SIO_000772 20806108 NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_provenance.
- NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_assertion wasDerivedFrom befree-20150227 NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_provenance.
- NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_assertion wasGeneratedBy ECO_0000203 NP275384.RAwzqgrL7c5gHn3CoYIfC9IA8tPx0RMvADO1D4Ar1ufBI130_provenance.