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- NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_assertion type Assertion NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_head.
- NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_assertion description "[Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_provenance.
- NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_assertion evidence source_evidence_curated NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_provenance.
- NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_assertion SIO_000772 15154116 NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_provenance.
- NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_assertion wasDerivedFrom ctd_human-20150221 NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_provenance.
- NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_assertion wasGeneratedBy ECO_0000218 NP34238.RAkQ6L_nOmsXIRuzyUtQQbnXZghEaVTGd78m155gOk39o130_provenance.