Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance.
- NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_assertion description "[The TNFA-1031T/T genotype was found to be associated with SSc (P < 0.0001) and both the DcSSc (diffuse subset of SSc) and the LcSSc (limited subset of SSc) subsets (P= 0.0004 and P= 0.0009, respectively) and the TNFA-237G/G genotype was found to be associated with all SSc (P= 0.0003) and with the DcSSc and LcSSc subsets (P= 0.01 and P= 0.005, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance.
- NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_assertion evidence source_evidence_literature NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance.
- NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_assertion SIO_000772 17498268 NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance.
- NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_assertion wasDerivedFrom gad-20130706 NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance.
- NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_assertion wasGeneratedBy ECO_0000203 NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance.
- gad-20130706 importedOn "2013-07-06" NP50294.RArjKfUdldx-XKhCMe_bcDETZ2oF4rQBEiKSQn4jiDZ_I130_provenance.