Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_assertion> ?p ?o ?g. }
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- NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_assertion type Assertion NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_head.
- NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_assertion description "[Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is a rare form of nonhypertensive cerebral small-vessel disease caused by mutations in the HTRA1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance.
- NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_assertion evidence source_evidence_literature NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance.
- NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_assertion SIO_000772 25712943 NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance.
- NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_assertion wasDerivedFrom befree-2016 NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance.
- NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_assertion wasGeneratedBy ECO_0000203 NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance.