Matches in Nanopublications for { ?s ?p "[One form of FTD-U, due to mutations in the valosin containing protein (VCP) gene, occurs with an inclusion body myopathy (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_assertion description "[One form of FTD-U, due to mutations in the valosin containing protein (VCP) gene, occurs with an inclusion body myopathy (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193553.RAWgqKelOEBxz20R47_zvF0755NSnYBfV5PrlD0aWDgzU130_provenance.
- assertion description "[One form of FTD-U, due to mutations in the valosin containing protein (VCP) gene, occurs with an inclusion body myopathy (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[One form of FTD-U, due to mutations in the valosin containing protein (VCP) gene, occurs with an inclusion body myopathy (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP693451.RAuNBlAk9ZIOROkG1i9ghDIm2PgddDkJP242Jr-at9PFc130_assertion description "[One form of FTD-U, due to mutations in the valosin containing protein (VCP) gene, occurs with an inclusion body myopathy (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693451.RAuNBlAk9ZIOROkG1i9ghDIm2PgddDkJP242Jr-at9PFc130_provenance.
- NP693445.RAKgWwbz9QRTD1NvcXe3iZOIaKIvucz9f9jO5PbdQrJwU130_assertion description "[One form of FTD-U, due to mutations in the valosin containing protein (VCP) gene, occurs with an inclusion body myopathy (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693445.RAKgWwbz9QRTD1NvcXe3iZOIaKIvucz9f9jO5PbdQrJwU130_provenance.
- NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_assertion description "[One form of FTD-U, due to mutations in the valosin containing protein (VCP) gene, occurs with an inclusion body myopathy (IBMPFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693449.RAzPOBKVmdhqwezexSqkcjAeQRHSPM3INEyZpBCUYTfys130_provenance.