Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_assertion> ?p ?o ?g. }
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- NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_assertion type Assertion NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_head.
- NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_assertion description "[Hereditary cystatin C amyloid angiopathy (HCCAA) is an autosomal dominant disorder in which a cysteine proteinase inhibitor, cystatin C, is deposited as amyloid fibrils in the cerebral arteries of patients and leads to massive brain haemorrhage and death in young adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_provenance.
- NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_assertion evidence source_evidence_literature NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_provenance.
- NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_assertion SIO_000772 2900981 NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_provenance.
- NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_assertion wasDerivedFrom befree-2016 NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_provenance.
- NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_assertion wasGeneratedBy ECO_0000203 NP1298180.RATwrZCtALXXfPcIxJDIHfOIvOFjnc2XSUJN0qP-forNc130_provenance.