Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance.
- NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_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." NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance.
- NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_assertion evidence source_evidence_literature NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance.
- NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_assertion SIO_000772 16821265 NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance.
- NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_assertion wasDerivedFrom befree-20150227 NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance.
- NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_assertion wasGeneratedBy ECO_0000203 NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP284938.RATq_DnmBc2lIYq6SantHREcK2EBQF-4R0eo9rlNU8tbc130_provenance.