Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_assertion> ?p ?o ?g. }
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- NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_assertion type Assertion NP642341.RAR3mUdAqwE96519yF2RTqp6ggQifVBpjyhXd9PNEuqd0130_head.
- 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.