Matches in Nanopublications for { ?s ?p "[Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 7 of
7
with 100 items per page.
- assertion description "[Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_assertion description "[Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797211.RAb0cBwKYOykIWNhZLFJFNdJDnaFnRevzB1nG6SNQ_1f0130_provenance.
- assertion description "[Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1135021.RAVSG690gZubinBC2dhzzFtuOYAqFakEjw6TooOzsnikk130_assertion description "[Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1135021.RAVSG690gZubinBC2dhzzFtuOYAqFakEjw6TooOzsnikk130_provenance.
- NP223173.RAi_NIdJxxs5mCrJdjAFa_z3etlFJbXZgCZbRGGkKOwLk130_assertion description "[Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223173.RAi_NIdJxxs5mCrJdjAFa_z3etlFJbXZgCZbRGGkKOwLk130_provenance.
- NP1135020.RAA5KUzf3D9wKtJvFldaE72xtDZLANqab5cZgRj_D1AJY130_assertion description "[Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1135020.RAA5KUzf3D9wKtJvFldaE72xtDZLANqab5cZgRj_D1AJY130_provenance.