Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance.
- NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_assertion description "[genetic variants investigated in this study may be associated with a moderate modification of the risk for AD in some samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance.
- NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_assertion evidence source_evidence_literature NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance.
- NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_assertion SIO_000772 17387528 NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance.
- NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_assertion wasDerivedFrom gad-20130706 NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance.
- NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_assertion wasGeneratedBy ECO_0000203 NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance.
- gad-20130706 importedOn "2013-07-06" NP64999.RAgsmazUGHdtIJZ6M4MjYOjPqROoto24iDaIWSRttLdhI130_provenance.