Matches in Nanopublications for { ?s ?p "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP475739.RACLzlc0XOqTjcgdJgJdmQJPaPYWaHvTkuCG-IRbK0C2I130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475739.RACLzlc0XOqTjcgdJgJdmQJPaPYWaHvTkuCG-IRbK0C2I130_provenance.
- NP696307.RAl9YxLHLArVnxrwqRR40Dtvk4qArmV5OPDhEPLO9to7A130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP696307.RAl9YxLHLArVnxrwqRR40Dtvk4qArmV5OPDhEPLO9to7A130_provenance.
- NP344979.RARq1lx6oB56z0mF19mpf9KX2FJlqmo_vndsVd8hM-JUI130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344979.RARq1lx6oB56z0mF19mpf9KX2FJlqmo_vndsVd8hM-JUI130_provenance.
- NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804668.RAi31DMPuG5OQpAhZdaXG_bhPS5Y5dwUwBgeq8WSO5-jM130_provenance.
- NP870585.RAbpj8zZZu1Yyjq1f9Kf4uskCAo1SbI6ovSV8IXsyVTCE130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870585.RAbpj8zZZu1Yyjq1f9Kf4uskCAo1SbI6ovSV8IXsyVTCE130_provenance.
- NP321896.RAG1x6qBaYdJLZzRC2VUkWtcTMDB6iphR5bha9JQ-3nsM130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321896.RAG1x6qBaYdJLZzRC2VUkWtcTMDB6iphR5bha9JQ-3nsM130_provenance.
- NP629631.RAzP4Lsm832TUZidGJsEJ7FU3xMBvDr13vdRtAeOGNAh4130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629631.RAzP4Lsm832TUZidGJsEJ7FU3xMBvDr13vdRtAeOGNAh4130_provenance.
- NP823487.RAyMge8KnexT8_WCdi7YmOQPvSqRBZyP1kuR0xGeipvv8130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823487.RAyMge8KnexT8_WCdi7YmOQPvSqRBZyP1kuR0xGeipvv8130_provenance.
- NP886970.RA3HytQjGdwnyhM8Uqp42EdpR3renkthUETuY0-ZyRTII130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886970.RA3HytQjGdwnyhM8Uqp42EdpR3renkthUETuY0-ZyRTII130_provenance.
- NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_assertion description "[Autosomal dominant proximal limb girdle or inclusion body myopathy, associated with Paget disease of bone and frontotemporal dementia (IBMPFD) is a recently described disorder that maps to chromosome 9p21.1-p12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731396.RAEkY3UmqklA1ePFY2GsLNWvnjzv-p59r896LTqvaL7ss130_provenance.