Matches in Nanopublications for { ?s ?p "[More recently, several heterozygous, homozygous or compound heterozygous mutations in the G protein-coupled prokineticin receptor-2 (PROKR2) and one of its ligands, prokineticin-2 (PROK2) were described in Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_assertion description "[More recently, several heterozygous, homozygous or compound heterozygous mutations in the G protein-coupled prokineticin receptor-2 (PROKR2) and one of its ligands, prokineticin-2 (PROK2) were described in Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584911.RAzI8E0keYz-ZTbgem1DJh4NddyyPWnJ5Tu-C8LwvKGWE130_provenance.
- assertion description "[More recently, several heterozygous, homozygous or compound heterozygous mutations in the G protein-coupled prokineticin receptor-2 (PROKR2) and one of its ligands, prokineticin-2 (PROK2) were described in Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[More recently, several heterozygous, homozygous or compound heterozygous mutations in the G protein-coupled prokineticin receptor-2 (PROKR2) and one of its ligands, prokineticin-2 (PROK2) were described in Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_assertion description "[More recently, several heterozygous, homozygous or compound heterozygous mutations in the G protein-coupled prokineticin receptor-2 (PROKR2) and one of its ligands, prokineticin-2 (PROK2) were described in Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619563.RA40AsGTjDqWUPPc3fSuVnwv0qDDt68AXl-R4DY3sBtU0130_provenance.
- NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_assertion description "[More recently, several heterozygous, homozygous or compound heterozygous mutations in the G protein-coupled prokineticin receptor-2 (PROKR2) and one of its ligands, prokineticin-2 (PROK2) were described in Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619564.RA_sunwtnCTImBj5Y9baijdd3ZEDBCGpPbyGLpcj6eXxg130_provenance.