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- source_evidence_literature type ECO_0000212 NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_provenance.
- NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_assertion description "[SNP mapping in the RUNX1 gene associated with RA in a Japanese population and a SUMO4 polymorphism associated with T1D were also studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_provenance.
- NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_assertion evidence source_evidence_literature NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_provenance.
- NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_assertion SIO_000772 16821265 NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_provenance.
- NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_assertion wasDerivedFrom befree-2016 NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_provenance.
- NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_assertion wasGeneratedBy ECO_0000203 NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_provenance.
- befree-2016 importedOn "2016-02-19" NP558236.RA_BaTrvO5YFBNB7NkDhlzdj_wk4x0APmAI8XH08ZbI4s130_provenance.