Matches in Nanopublications for { ?s ?p "[Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP25907.RATBwb6vScOE654lnm9wZqm6PLMNRvp4CjMNiFlJOXK0w130_assertion description "[Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25907.RATBwb6vScOE654lnm9wZqm6PLMNRvp4CjMNiFlJOXK0w130_provenance.
- NP25741.RAcrUrQIRAy91Zq0lHsIc_SJFgI3rmTrNF_YLGsrTFHNU130_assertion description "[Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25741.RAcrUrQIRAy91Zq0lHsIc_SJFgI3rmTrNF_YLGsrTFHNU130_provenance.
- assertion description "[Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP13503.RARMYkxRtEmJfPihRUySN8Qb7EvK1awGP3nx-XZFXpGhM130_assertion description "[Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13503.RARMYkxRtEmJfPihRUySN8Qb7EvK1awGP3nx-XZFXpGhM130_provenance.
- NP420011.RACph2Cl1MCtx5XjhSz6rg5CekQknuio0b92MOISL-plU130_assertion description "[Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420011.RACph2Cl1MCtx5XjhSz6rg5CekQknuio0b92MOISL-plU130_provenance.