Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance.
- NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_assertion description "[Most probably the lack of mutated SLC22A4 substrate explains the absence of RUNX1 association with RA observed in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance.
- NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_assertion evidence source_evidence_literature NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance.
- NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_assertion SIO_000772 16652416 NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance.
- NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_assertion wasDerivedFrom befree-20140225 NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance.
- NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_assertion wasGeneratedBy ECO_0000203 NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP274081.RABIsrLTssVNeTCqnjS9GqzX55cOjLQ4ldmipF9Z8leXg130_provenance.