Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance.
- NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_assertion description "[MEFV, and particularly the E148Q mutation, is an independent modifier of the clinical manifestations of RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance.
- NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_assertion evidence source_evidence_literature NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance.
- NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_assertion SIO_000772 15958759 NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance.
- NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_assertion wasDerivedFrom befree-20140225 NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance.
- NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_assertion wasGeneratedBy ECO_0000203 NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_provenance.