Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance.
- NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_assertion description "[Hereditary angioedema (HAE) due to C1 inhibitor (C1-INH) deficiency is a rare genetic disease characterized by recurrent swellings of the subcutaneous and submucosal tissues that can manifest as cutaneous edema, abdominal pain and laryngeal edema with airway obstruction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance.
- NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_assertion evidence source_evidence_literature NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance.
- NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_assertion SIO_000772 23634741 NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance.
- NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_assertion wasDerivedFrom befree-20150227 NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance.
- NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_assertion wasGeneratedBy ECO_0000203 NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP275322.RARbfsP1vxcGFZ20jJ8YnbYlomagGLrPU_JVIGKAvAnyQ130_provenance.