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- NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_assertion type Assertion NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_head.
- NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_assertion wasGeneratedBy ECO_0000203 NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_provenance.
- NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_assertion wasDerivedFrom befree-20150227 NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_provenance.
- NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_assertion SIO_000772 12044915 NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_provenance.
- NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_assertion evidence source_evidence_literature NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_provenance.
- NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_assertion description "[Mutations in the StAR gene were found to be the cause of the potentially lethal disease in humans known as congenital lipoid adrenal hyperplasia (lipoid CAH), a condition characterized by an almost complete inability of the newborn to synthesize steroids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961165.RAd26O9ODJsN226-UE7G3FKLsUAWj6vtWYYPcruirOx6M130_provenance.