Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance.
- NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_assertion description "[The results of this study suggest that MEFV gene mutations appear to be an aggravating factor for the severity of RA, and consequently, patients with RA might be screened for MEFV gene mutations in countries where FMF is frequent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance.
- NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_assertion evidence source_evidence_literature NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance.
- NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_assertion SIO_000772 20031469 NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance.
- NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_assertion wasDerivedFrom befree-2016 NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance.
- NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_assertion wasGeneratedBy ECO_0000203 NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance.
- befree-2016 importedOn "2016-02-19" NP783220.RAEwHD0spL0c-lV_fQda9NV-8iS8IidqbqewQJoGZ8Qho130_provenance.