Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP764313.RAoiqLWH1qlwJLJ0Y38heBoeBGyDAyKlC97-PuaLhtNCo130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764313.RAoiqLWH1qlwJLJ0Y38heBoeBGyDAyKlC97-PuaLhtNCo130_provenance.
• NP510654.RAX7NmOIrha-V--mg4-9AQhLl_UimZv80IyouP1wrJaz0130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP510654.RAX7NmOIrha-V--mg4-9AQhLl_UimZv80IyouP1wrJaz0130_provenance.
• NP723934.RAdZE7MsKIgzhVE4fi3zq5HVf0MzhzpMabjdQ-B82qyK0130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723934.RAdZE7MsKIgzhVE4fi3zq5HVf0MzhzpMabjdQ-B82qyK0130_provenance.
• NP369370.RAS4b6e9AFdM2ElezKsSpF2ckMy-NsvEgzW5MqHkubj1Q130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP369370.RAS4b6e9AFdM2ElezKsSpF2ckMy-NsvEgzW5MqHkubj1Q130_provenance.
• NP266453.RArXPog2LyA6oVoKRwkZEOzAub6HXEU-_qhzA1-PRjZGA130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266453.RArXPog2LyA6oVoKRwkZEOzAub6HXEU-_qhzA1-PRjZGA130_provenance.
• NP926890.RAR0Zv_ewXqUT2TZNh53XHBHqWdyv342fIauqdBUWxNZE130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926890.RAR0Zv_ewXqUT2TZNh53XHBHqWdyv342fIauqdBUWxNZE130_provenance.
• NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622720.RA-PuFSWLeot-b_KtcreW-8XaC6Hj_0scOWVo9wo9olN8130_provenance.
• NP450127.RAtT3ZBIwy937i2cl1cpTsLlMgi5_09PmcQWCm5lYgErk130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450127.RAtT3ZBIwy937i2cl1cpTsLlMgi5_09PmcQWCm5lYgErk130_provenance.
• NP866713.RAc7ZG8qqIxkipr-7qjIO1mBO54fiBoDEKY1z61UBlWQ8130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866713.RAc7ZG8qqIxkipr-7qjIO1mBO54fiBoDEKY1z61UBlWQ8130_provenance.
• NP265753.RA1P2MdGU-qZzfMdwhEaZeHP2TzKsudUY-mRsViJztsc4130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265753.RA1P2MdGU-qZzfMdwhEaZeHP2TzKsudUY-mRsViJztsc4130_provenance.
• NP827808.RA1zg1bNb9v__ai5wL8J5jWHZgD7q1b1Ej4Vb-j5KhYTs130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827808.RA1zg1bNb9v__ai5wL8J5jWHZgD7q1b1Ej4Vb-j5KhYTs130_provenance.
• assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988522.RASbwn71FC_L73Ed0lhKpnybo_nQTT4FJFOQDW1v-me54130_provenance.
• NP919850.RA0TQqYPacNTfVpq0d6kA4886DfmukgFGkdULUsCjWdfA130_assertion description "[Hyperphosphatasia with mental retardation syndrome (HPMRS), an autosomal-recessive form of intellectual disability characterized by facial dysmorphism, seizures, brachytelephalangy, and persistent elevated serum alkaline phosphatase (hyperphosphatasia), was recently shown to be caused by mutations in PIGV, a member of the glycosylphosphatidylinositol (GPI)-anchor-synthesis pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919850.RA0TQqYPacNTfVpq0d6kA4886DfmukgFGkdULUsCjWdfA130_provenance.