Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_assertion> ?p ?o ?g. }
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- NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_assertion type Assertion NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_head.
- NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_assertion description "[Mutations in the KAL gene (Kallmann syndrome) and the AHC gene (adrenal hypoplasia congenita/HH) cause X-linked recessive HH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_provenance.
- NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_assertion evidence source_evidence_literature NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_provenance.
- NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_assertion SIO_000772 10727999 NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_provenance.
- NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_assertion wasDerivedFrom befree-20140225 NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_provenance.
- NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_assertion wasGeneratedBy ECO_0000203 NP305410.RAwfp8cPoPV_-c0kSnSmaeGKizkE15qzKDdMsJjx_aRwQ130_provenance.