Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

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• NP709536.RAqzliWcWjjnDwqDB0OEgzwdzuG_J4N4LziRlS3MG57Ew130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709536.RAqzliWcWjjnDwqDB0OEgzwdzuG_J4N4LziRlS3MG57Ew130_provenance.
• NP458655.RAvKsnahyeJcU-u3hPBJu1jwLcGjmVKR4WYrZFaCPN-tU130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP458655.RAvKsnahyeJcU-u3hPBJu1jwLcGjmVKR4WYrZFaCPN-tU130_provenance.
• assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP408918.RAYxrgMp3Xs3QEmCfaPvEN9py76SAuirBFnemJ5vnkMpM130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408918.RAYxrgMp3Xs3QEmCfaPvEN9py76SAuirBFnemJ5vnkMpM130_provenance.
• assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.
• NP1313708.RASXuhAWb5I1PW2YOL0lFfeWAX1CP6A5h5WsoZvQCHm4A130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313708.RASXuhAWb5I1PW2YOL0lFfeWAX1CP6A5h5WsoZvQCHm4A130_provenance.
• NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_provenance.
• NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_provenance.
• NP412420.RAKnZHQlWoDmrv2wiuHuPSEL-JPYxC4DGVptJyVE6yV4c130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412420.RAKnZHQlWoDmrv2wiuHuPSEL-JPYxC4DGVptJyVE6yV4c130_provenance.
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