Matches in Nanopublications for { ?s ?p "[Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP841730.RAgeP-CcfQnMEHOAqMw-IViB3v3lg0TgQ1HIvpLA3BLh4130_assertion description "[Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841730.RAgeP-CcfQnMEHOAqMw-IViB3v3lg0TgQ1HIvpLA3BLh4130_provenance.
- NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_assertion description "[Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_provenance.
- NP450190.RAMoyr4s71mAZ6QdAvTWLxup2KKOsRCrbbaJzyz53xmqw130_assertion description "[Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450190.RAMoyr4s71mAZ6QdAvTWLxup2KKOsRCrbbaJzyz53xmqw130_provenance.