Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_assertion> ?p ?o ?g. }
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- NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_assertion type Assertion NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_head.
- 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.