Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_assertion> ?p ?o ?g. }
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- NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_assertion type Assertion NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_head.
- 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.
- NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_assertion evidence source_evidence_literature NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_provenance.
- NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_assertion SIO_000772 15223798 NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_provenance.
- NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_assertion wasDerivedFrom befree-2016 NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_provenance.
- NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_assertion wasGeneratedBy ECO_0000203 NP450189.RAmIABElynzKZ3j9TaaLznTOqskBMnuGtfqvmF2AXUDN0130_provenance.