Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance.
- NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_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." NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance.
- NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_assertion evidence source_evidence_literature NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance.
- NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_assertion SIO_000772 17387528 NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance.
- NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_assertion wasDerivedFrom gad-20150221 NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance.
- NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_assertion wasGeneratedBy ECO_0000203 NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP106376.RADnFRpXoIvhz1Nr1ugGv53HQezF9GtM3r22tCFK1kglo130_provenance.