Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance.
- NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_assertion description "[Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance.
- NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_assertion evidence source_evidence_literature NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance.
- NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_assertion SIO_000772 21901158 NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance.
- NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_assertion wasDerivedFrom gad-20130706 NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance.
- NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_assertion wasGeneratedBy ECO_0000203 NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance.
- gad-20130706 importedOn "2013-07-06" NP96432.RAFIMxwuJUFeHI1Cwc92KY2fcVi6eu8i06HFSkRNoLgVE130_provenance.