Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance.
- NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_assertion description "[Although causal variants remain to be identified, our results demonstrate the existence of multiple GD susceptibility loci within the MHC region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance.
- NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_assertion evidence source_evidence_literature NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance.
- NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_assertion SIO_000772 21900946 NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance.
- NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_assertion wasDerivedFrom befree-20140225 NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance.
- NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_assertion wasGeneratedBy ECO_0000203 NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP237331.RAGyrl5Ms70XrKFa8GJwYFOnjXfYd83hYorFUHEkUIqf4130_provenance.