Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations of the KAL1 gene are a known cause of Kallmann syndrome, a disorder characterized by the coexistence of hypogonadotropic hypogonadism and anosmia/hiposmia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Loss-of-function mutations of the KAL1 gene are a known cause of Kallmann syndrome, a disorder characterized by the coexistence of hypogonadotropic hypogonadism and anosmia/hiposmia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_assertion description "[Loss-of-function mutations of the KAL1 gene are a known cause of Kallmann syndrome, a disorder characterized by the coexistence of hypogonadotropic hypogonadism and anosmia/hiposmia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231969.RAIbu0nDmCvW6_EaBUI4vzeZnjO14mJpy1pZsXGkXE16U130_provenance.