Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance.
- NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_assertion description "[The finding suggests that a point mutation in ND2 is a potential risk factor for Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance.
- NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_assertion evidence source_evidence_literature NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance.
- NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_assertion SIO_000772 1370613 NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance.
- NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_assertion wasDerivedFrom befree-20140225 NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance.
- NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_assertion wasGeneratedBy ECO_0000203 NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651153.RAO3PjajFTBIXSkkx3U6KRRm17HOjOplvAzmbEF99GI1A130_provenance.