Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion> ?p ?o ?g. }
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- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion type Assertion NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_head.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion description "[Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion evidence source_evidence_literature NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion SIO_000772 22152678 NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion wasDerivedFrom befree-20150227 NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion wasGeneratedBy ECO_0000203 NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.