Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance.
- befree-2016 importedOn "2016-02-19" NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance.
- NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_assertion wasGeneratedBy ECO_0000203 NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance.
- NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_assertion wasDerivedFrom befree-2016 NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance.
- NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_assertion SIO_000772 10818499 NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance.
- NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_assertion evidence source_evidence_literature NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance.
- NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_assertion description "[Even within patient groups with the same ApoE genotype (specifically, E4/4 homozygotes and E3/3 homozygotes), our recent analyses have found significant increases in VLs in association with severe CAA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284432.RAh3_gEGLuGDyAg2ksBUqUZa1rPW6rMLH9ye6EZiEGyTk130_provenance.