Matches in Nanopublications for { ?s ?p "[The novel variants that were observed only in the infertile cohort included the SNP c.65G>A mutation which resulted in an amino acid change at the codon 22 (p.Ser22Asn) in the PRM1 gene, a mutation in the promoter region of PRM2 (-67C>T) and a nonsense mutation in the PRM3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP821903.RABJYsngnhiwdu5AN5mOBFKykowYR-rkkXnAqUzLgR0Mk130_assertion description "[The novel variants that were observed only in the infertile cohort included the SNP c.65G>A mutation which resulted in an amino acid change at the codon 22 (p.Ser22Asn) in the PRM1 gene, a mutation in the promoter region of PRM2 (-67C>T) and a nonsense mutation in the PRM3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821903.RABJYsngnhiwdu5AN5mOBFKykowYR-rkkXnAqUzLgR0Mk130_provenance.
- NP561347.RAnga3HtRSLMU4JHQGeiYlNViGiDWZ7HawcQcv1YpHPxc130_assertion description "[The novel variants that were observed only in the infertile cohort included the SNP c.65G>A mutation which resulted in an amino acid change at the codon 22 (p.Ser22Asn) in the PRM1 gene, a mutation in the promoter region of PRM2 (-67C>T) and a nonsense mutation in the PRM3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561347.RAnga3HtRSLMU4JHQGeiYlNViGiDWZ7HawcQcv1YpHPxc130_provenance.
- NP209076.RAIunRd1owhpA1GOfquvIkCkPQtpo771fkLLH24__7Qzg130_assertion description "[The novel variants that were observed only in the infertile cohort included the SNP c.65G>A mutation which resulted in an amino acid change at the codon 22 (p.Ser22Asn) in the PRM1 gene, a mutation in the promoter region of PRM2 (-67C>T) and a nonsense mutation in the PRM3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209076.RAIunRd1owhpA1GOfquvIkCkPQtpo771fkLLH24__7Qzg130_provenance.