Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance.
- NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_assertion description "[Although certain inherited forms of CAA with cerebral haemorrhage are associated with autosomal dominant mutations in APP and other genes (cystatin-C, transthyretin, gelsolin, ABrit, ADan), in most cases of AD CAA does not associate clearly with any genetic risk factor other than APO E beta4 allele, which appears to increase the severity of CAA in a dose dependent manner, especially within the occipital cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance.
- NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_assertion evidence source_evidence_literature NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance.
- NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_assertion SIO_000772 15876981 NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance.
- NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_assertion wasDerivedFrom befree-2016 NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance.
- NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_assertion wasGeneratedBy ECO_0000203 NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance.
- befree-2016 importedOn "2016-02-19" NP493451.RAkb4PuA7csvkX7cadELtAZpySF0DfVYnOC2Ca4H_HFVI130_provenance.