Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance.
- NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_assertion description "[Genetic variation at PNPLA3 confers a markedly increased risk of increasingly severe histological features of NAFLD, without a strong effect on metabolic syndrome component traits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance.
- NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_assertion evidence source_evidence_literature NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance.
- NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_assertion SIO_000772 20648472 NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance.
- NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_assertion wasDerivedFrom gad-20150221 NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance.
- NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_assertion wasGeneratedBy ECO_0000203 NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP182033.RAXQ-T-3go-DdMg_UXW7CGQ-mHPmecR7b10vsDVPSsXVw130_provenance.