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- source_evidence_literature type ECO_0000212 NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_provenance.
- NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_assertion description "[Therefore, in this present study, we find no evidence for the involvement of this polymorphism either in increasing the susceptibility to AD, or by acting as a phenotypic modifier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_provenance.
- NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_assertion evidence source_evidence_literature NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_provenance.
- NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_assertion SIO_000772 15925094 NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_provenance.
- NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_assertion wasDerivedFrom gad-20150221 NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_provenance.
- NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_assertion wasGeneratedBy ECO_0000203 NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69481.RAbYmeQl5slRimLl8WtFfGn2MDx69SJk2374z_PcjlopE130_provenance.