Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance.
- NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_assertion description "[Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance.
- NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_assertion evidence source_evidence_curated NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance.
- NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_assertion SIO_000772 2111584 NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance.
- NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_assertion wasDerivedFrom uniprot-2016 NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance.
- NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_assertion wasGeneratedBy ECO_0000218 NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6446.RAkl_0nOrV7oNh2stScxUFu5DvSProO20XmVI59KSvX-o130_provenance.