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- source_evidence_literature type ECO_0000212 NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_provenance.
- NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_assertion description "[Our study replicated previous GWAS findings for markers in VAX1 in the Asian population, and identified rare variants in PAX7 and VAX1 that may contribute to the etiology of CL(P).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_provenance.
- NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_assertion evidence source_evidence_literature NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_provenance.
- NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_assertion SIO_000772 23463464 NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_provenance.
- NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_assertion wasDerivedFrom befree-2016 NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_provenance.
- NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_assertion wasGeneratedBy ECO_0000203 NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_provenance.
- befree-2016 importedOn "2016-02-19" NP1058079.RAkapkK_7arcEljqGyIM1a50Van-71l4XRQqpoTyT_W60130_provenance.