Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.
- NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_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." NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.
- NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_assertion evidence source_evidence_curated NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.
- NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_assertion SIO_000772 10739753 NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.
- NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_assertion wasDerivedFrom ctd_human-2016 NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.
- NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_assertion wasGeneratedBy ECO_0000218 NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.