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- NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_assertion type Assertion NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_head.
- NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_assertion wasGeneratedBy ECO_0000203 NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_provenance.
- NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_assertion wasDerivedFrom befree-2016 NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_provenance.
- NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_assertion SIO_000772 19551906 NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_provenance.
- NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_assertion evidence source_evidence_literature NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_provenance.
- NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_assertion description "[Leydig cell hypoplasia (LCH) is a rare form of male pseudohermaphroditism caused by inactivating mutations in the luteinizing hormone receptor gene (LHCGR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747298.RAku3vgTs23a8ts1nCV1SckmSv95CLjsqrsZ6WtYQj-tw130_provenance.