Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_assertion> ?p ?o ?g. }
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- NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_assertion type Assertion NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_head.
- NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_assertion wasGeneratedBy ECO_0000203 NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_provenance.
- NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_assertion wasDerivedFrom befree-20150227 NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_provenance.
- NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_assertion SIO_000772 12044915 NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_provenance.
- NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_assertion evidence source_evidence_literature NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_provenance.
- NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_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." NP961111.RA3ps4cw9MQVujNQahEQmFQzHr9lkw8cBh0pVGfrWFzPc130_provenance.