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- NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_assertion type Assertion NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_head.
- NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_assertion description "[This mutation was recently described in a family of Italian descent with CVT and Charcot-Marie-Tooth deformity HOXD10 gene mutations were not identified in any of the other families or sporadic patients with CVT, suggesting that genetic heterogeneity underlies this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_provenance.
- NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_assertion evidence source_evidence_literature NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_provenance.
- NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_assertion SIO_000772 16450407 NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_provenance.
- NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_assertion wasDerivedFrom befree-2016 NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_provenance.
- NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_assertion wasGeneratedBy ECO_0000203 NP533944.RAdtv5NEteQ0-D0fLfZ6mgMOHlZuoIO5bLzEnPXpDPWiI130_provenance.