Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance.
- NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_assertion description "[Although our study covers common variants across the NAMPT gene, the possible involvement of rare variants in T2DM etiology cannot be ruled out and will require the investigation of very large numbers of cases and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance.
- NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_assertion evidence source_evidence_literature NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance.
- NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_assertion SIO_000772 20451405 NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance.
- NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_assertion wasDerivedFrom befree-20140225 NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance.
- NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_assertion wasGeneratedBy ECO_0000203 NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP210200.RA7MnXPRYOJuVTe08L5ZlntMwUngq3Tw7bPlVuR1u1Grg130_provenance.