Matches in Nanopublications for { ?s ?p "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231373.RA0XdLrdSGkzd7D_77d0RuEWI9g8EvEXZF8nl-ABu43jM130_provenance.
- NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13098.RASf3OFQEJMbkQT5LMwpkjJBaayAFIz_Z_-iJ88gYBnu4130_provenance.
- NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977255.RAb8tM2x3o5Xtw00uKzZccCtL6eNGpH1gkZDbwDRJNSWE130_provenance.
- assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_assertion description "[In humans, we identified recessive loss-of-function DYX1C1 mutations in 12 individuals with PCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1095422.RAPmUJ3ONBEfib9CJjvUIv5IN1i74a4uWGGEddnFTKTi0130_provenance.