Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance.
- NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_assertion description "[Renal insufficiency in non-diabetic subjects is explained by interactions of MTHFR C677T polymorphism mutation with LVH, hsCRP, intact parathyroid hormone (iPTH), and RRI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance.
- NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_assertion evidence source_evidence_literature NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance.
- NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_assertion SIO_000772 23534584 NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance.
- NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_assertion wasDerivedFrom befree-20140225 NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance.
- NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_assertion wasGeneratedBy ECO_0000203 NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP538266.RA-0QFfC16uH2Vn-p0l47gymmwThdLN2Kpa0LinivE63s130_provenance.