Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.
- NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.
- NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_assertion evidence source_evidence_curated NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.
- NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_assertion SIO_000772 10739753 NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.
- NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_assertion wasDerivedFrom ctd_human-2016 NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.
- NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_assertion wasGeneratedBy ECO_0000218 NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.