Matches in Nanopublications for { ?s ?p "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP748249.RADO-NwxInOJaCkmjtCOoZuXL6swi9h8bVHM8mNJ5UEPc130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748249.RADO-NwxInOJaCkmjtCOoZuXL6swi9h8bVHM8mNJ5UEPc130_provenance.
- NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478342.RAcZTK7Z0Hov7vjBQYuuqQuq3PNjYgYxUSnnvtaRJ1niY130_provenance.
- NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_provenance.
- NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939775.RAfSCbEnpQCte4H-ASrJvUSpGyBgaJb4lBJ-OnZaL9VoQ130_provenance.
- assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502624.RAhU1GPb7TAFbaEiD7va7aCK4dNsDkyqIlRhMAVkarNKc130_provenance.
- NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502625.RAp3rPopBruIBrpwr-VnEU1knGul2snWxhi9qVaoo0pBQ130_provenance.
- NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838648.RA2iQTNoDwNp2mo_O2y2LiEWWDtc5MofERe83uT_BM8jU130_provenance.