Matches in Nanopublications for { ?s ?p "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 12 of
12
with 100 items per page.
- NP148933.RAmlVDYLEHBLKCPNuz7PN5GHasDVVpcAoD7BUVqiwZUhA130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148933.RAmlVDYLEHBLKCPNuz7PN5GHasDVVpcAoD7BUVqiwZUhA130_provenance.
- NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141014.RABMPnw6lRlUWzoBQlR_ajg4PiKa_vxoTe6WC353oFMUs130_provenance.
- NP134965.RAiWloxe7KsFBp9O7pkhIqznQDZfImSqmxCS1O0Agcmqo130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134965.RAiWloxe7KsFBp9O7pkhIqznQDZfImSqmxCS1O0Agcmqo130_provenance.
- NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204158.RACRS9EaTVOTGSgwM_WCQZvmSOV9ePq66YBOgFCnHwRGc130_provenance.
- NP192736.RAcuyhMMgjTvAKdIN97DVoGYBLoGO3Tyz3hPZ26Qce4pQ130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192736.RAcuyhMMgjTvAKdIN97DVoGYBLoGO3Tyz3hPZ26Qce4pQ130_provenance.
- assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198122.RAoo5HOwSKu2yI4PRhgZmy-w_KO7a2ad5H0Rwr4_P6IuM130_provenance.
- NP212058.RAroW73NwvvXOkY9B3za8xSspWsTpt81gYHaBNNgQzLdA130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212058.RAroW73NwvvXOkY9B3za8xSspWsTpt81gYHaBNNgQzLdA130_provenance.
- NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192737.RAq8TcZ5YeFZNWbeUhGISCQlyCMyTYG8tc5MQ9YqBearU130_provenance.
- NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_provenance.