Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance.
- NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_assertion description "[An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance.
- NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_assertion evidence source_evidence_curated NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance.
- NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_assertion SIO_000772 8048949 NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance.
- NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_assertion wasDerivedFrom ctd_human-2016 NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance.
- NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_assertion wasGeneratedBy ECO_0000218 NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP36863.RAdmtYhGO8WZllHtUGLirLhCC36p7cs1Gtm_yLlryNTvY130_provenance.