Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance.
- NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_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." NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance.
- NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_assertion evidence source_evidence_curated NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance.
- NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_assertion SIO_000772 2111584 NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance.
- NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_assertion wasDerivedFrom ctd_human-20130708 NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance.
- NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_assertion wasGeneratedBy ECO_0000218 NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP8969.RAnyFygufmaDIV3HvWtDRbYKfspBwzByNNnb-TWLTBhDI130_provenance.