Matches in Nanopublications for { ?s ?p "[Achondroplasia (ACH) is the most common form of osteochondrodysplasia, and is mostly associated with a point mutation in the gene on the transmembrane domain of fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP673327.RAvGw8AiES79mUt9ppKHsjG2uHkfp78ANuAecs20luSfU130_assertion description "[Achondroplasia (ACH) is the most common form of osteochondrodysplasia, and is mostly associated with a point mutation in the gene on the transmembrane domain of fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673327.RAvGw8AiES79mUt9ppKHsjG2uHkfp78ANuAecs20luSfU130_provenance.
- NP492642.RAZ24nkTriWRLVAcMW1ufLIJc-nKcYcRATCHcqHQvqxBs130_assertion description "[Achondroplasia (ACH) is the most common form of osteochondrodysplasia, and is mostly associated with a point mutation in the gene on the transmembrane domain of fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492642.RAZ24nkTriWRLVAcMW1ufLIJc-nKcYcRATCHcqHQvqxBs130_provenance.
- assertion description "[Achondroplasia (ACH) is the most common form of osteochondrodysplasia, and is mostly associated with a point mutation in the gene on the transmembrane domain of fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1404361.RAX8iXrVi2Le28DDRMiLZdDanIJmbkYVik8ohcLcxApdw130_assertion description "[Achondroplasia (ACH) is the most common form of osteochondrodysplasia, and is mostly associated with a point mutation in the gene on the transmembrane domain of fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404361.RAX8iXrVi2Le28DDRMiLZdDanIJmbkYVik8ohcLcxApdw130_provenance.
- NP400981.RApgi3YYjSFKXijc5BNZLDFevx8yIku8f8mjzEE-FeppE130_assertion description "[Achondroplasia (ACH) is the most common form of osteochondrodysplasia, and is mostly associated with a point mutation in the gene on the transmembrane domain of fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400981.RApgi3YYjSFKXijc5BNZLDFevx8yIku8f8mjzEE-FeppE130_provenance.
- NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_assertion description "[Achondroplasia (ACH) is the most common form of osteochondrodysplasia, and is mostly associated with a point mutation in the gene on the transmembrane domain of fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404360.RAuPMgRHrpVzbcjUwH8OJN1MENbx8orH4719HjU304Stw130_provenance.
- NP400962.RA7IdN8jE3LcUOtM6Ak8J2q_1yqzjp56Ohs80DfpC5YlY130_assertion description "[Achondroplasia (ACH) is the most common form of osteochondrodysplasia, and is mostly associated with a point mutation in the gene on the transmembrane domain of fibroblast growth factor receptor-3 (FGFR-3) on chromosome 4p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400962.RA7IdN8jE3LcUOtM6Ak8J2q_1yqzjp56Ohs80DfpC5YlY130_provenance.