Matches in Nanopublications for { ?s ?p "[Genetic linkage analysis and mutation studies have identified CYP1B1 as a causative gene in PCG, as a modifier gene in POAG, and, on rare occasions, as causative gene in POAG as well as in several ASD disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_assertion description "[Genetic linkage analysis and mutation studies have identified CYP1B1 as a causative gene in PCG, as a modifier gene in POAG, and, on rare occasions, as causative gene in POAG as well as in several ASD disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
- assertion description "[Genetic linkage analysis and mutation studies have identified CYP1B1 as a causative gene in PCG, as a modifier gene in POAG, and, on rare occasions, as causative gene in POAG as well as in several ASD disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_assertion description "[Genetic linkage analysis and mutation studies have identified CYP1B1 as a causative gene in PCG, as a modifier gene in POAG, and, on rare occasions, as causative gene in POAG as well as in several ASD disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633561.RAQ_dtpxoedj8Gy8DUx02SirakQOr2FMQWjlV1kt2kAbc130_provenance.