Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance.
- NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_assertion description "[However, the GG genotype of the MIF SNP rs1007888 was associated with MI in Czech female patients (p=0.027).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance.
- NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_assertion evidence source_evidence_literature NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance.
- NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_assertion SIO_000772 19167373 NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance.
- NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_assertion wasDerivedFrom befree-20140225 NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance.
- NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_assertion wasGeneratedBy ECO_0000203 NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP446573.RABhEjq4f_JEc23QfG95xiKGQg6TPwvkM8kcaE-E_iLq4130_provenance.