Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.]. 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 in FGFR1 cause autosomal dominant Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP386333.RAq9K30LALLcPkOzKYmbNcJ9t76tmpQkfg6Q6zp-KsCkM130_assertion description "[Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386333.RAq9K30LALLcPkOzKYmbNcJ9t76tmpQkfg6Q6zp-KsCkM130_provenance.
- NP2557.RAwere2hhN-LXBYHMbnV9k-HW0FD0ZqN-6bsuWDgIicfc130_assertion description "[Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2557.RAwere2hhN-LXBYHMbnV9k-HW0FD0ZqN-6bsuWDgIicfc130_provenance.