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- NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_assertion type Assertion NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_head.
- NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_assertion description "[Recently, another causative gene, CISD2, has been identified in patients with a type of Wolfram syndrome (WS2) resulting in early optic atrophy, diabetes mellitus, deafness, decreased lifespan, but not diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_provenance.
- NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_assertion evidence source_evidence_literature NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_provenance.
- NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_assertion SIO_000772 22790102 NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_provenance.
- NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_assertion wasDerivedFrom befree-20140225 NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_provenance.
- NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_assertion wasGeneratedBy ECO_0000203 NP650217.RATjCUlioN-WHsvMs0ymEMQ2Y2RcDFawDHZ_17MTetDsI130_provenance.