Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance.
- NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_assertion description "[We postulate that to fully determine whether the sequence differences in VDR gene are susceptibility variants for T2DM, additional studies in different populations are required in a large study group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance.
- NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_assertion evidence source_evidence_literature NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance.
- NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_assertion SIO_000772 14714273 NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance.
- NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_assertion wasDerivedFrom befree-2016 NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance.
- NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_assertion wasGeneratedBy ECO_0000203 NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance.
- befree-2016 importedOn "2016-02-19" NP427364.RAcXbykPf3oskLp2KZeHN07zyXDJICv3xllAW5wlLmRJM130_provenance.