Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance.
- NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_assertion description "[The results suggested that the 866C-->T polymorphism might be associated with PE and EH. It is plausible that apo J may play a certain role in the predisposition to PE and EH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance.
- NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_assertion evidence source_evidence_literature NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance.
- NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_assertion SIO_000772 15925890 NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance.
- NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_assertion wasDerivedFrom gad-20150221 NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance.
- NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_assertion wasGeneratedBy ECO_0000203 NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92994.RAiMec8y0PljQ2l88StfaoEOQfWR_StdgR-UBS04DUrpI130_provenance.