Matches in Nanopublications for { ?s ?p "[Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_assertion description "[Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5004.RARUN1zsO2OhrTEgcjxsEWzJ1sQnR0EqcIQEwfM6uuC2g130_provenance.
- assertion description "[Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_assertion description "[Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7435.RADI14khpex7oWYn2cM28YYlguIn1Mgt05OvN6moOpsw4130_provenance.