Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_assertion> ?p ?o ?g. }
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- NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_assertion type Assertion NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_head.
- NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_assertion description "[Hereditary angioedema (HAE) is characterized by a deficiency in C1 inhibitor protein (C1 INH) and by clinical symptoms of episodic swelling of subcutaneous or mucosal tissue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_provenance.
- NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_assertion evidence source_evidence_literature NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_provenance.
- NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_assertion SIO_000772 1595700 NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_provenance.
- NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_assertion wasDerivedFrom befree-2016 NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_provenance.
- NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_assertion wasGeneratedBy ECO_0000203 NP499580.RAXNznRYVpVHGNaRTFZd52p90bqRToXRHkZtYn_eZvuiY130_provenance.