Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1266137.RAfyHO9ADZx7m5ud3omCKmb-USycGdmCABQ5rfjCWL9ik130_provenance.