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- source_evidence_literature type ECO_0000212 NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_provenance.
- NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_assertion description "[The coding regions of EIF2AK3 were sequenced in 34 probands with infancy-onset diabetes with a clinical phenotype suggestive of WRS (n = 28) or homozygosity at the WRS locus (n = 6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_provenance.
- NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_assertion evidence source_evidence_literature NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_provenance.
- NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_assertion SIO_000772 19837917 NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_provenance.
- NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_assertion wasDerivedFrom befree-20140225 NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_provenance.
- NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_assertion wasGeneratedBy ECO_0000203 NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP391357.RAKnbdZHDOi-5shp_0GZ25oCNVvkt6udO-lw1G5a73Jn0130_provenance.