Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_assertion> ?p ?o ?g. }
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- NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_assertion type Assertion NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_head.
- NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_assertion description "[Familial cerebral cavernous malformation type 1 (CCM1) is an autosomal dominant disease caused by mutations in the Krev Interaction Trapped 1 (KRIT1/CCM1) gene, and characterized by multiple brain lesions that often result in intracerebral hemorrhage (ICH), seizures, and neurological deficits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_provenance.
- NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_assertion evidence source_evidence_literature NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_provenance.
- NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_assertion SIO_000772 25472749 NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_provenance.
- NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_assertion wasDerivedFrom befree-2016 NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_provenance.
- NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_assertion wasGeneratedBy ECO_0000203 NP1244636.RAtJE9GXznJlLxPN9Jp-MpWGFANMQDfYFtnb0Ha6bc7d8130_provenance.