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- NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_assertion type Assertion NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_head.
- NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_assertion description "[While double knockout of Dlx5 and Dlx6 resulted in limb defects in mice, the majority of patients with SHFM1 had only heterozygous chromosomal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_provenance.
- NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_assertion evidence source_evidence_literature NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_provenance.
- NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_assertion SIO_000772 25332435 NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_provenance.
- NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_assertion wasDerivedFrom befree-2016 NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_provenance.
- NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_assertion wasGeneratedBy ECO_0000203 NP1231035.RAd843aU1LeJTmkupH4BBgy3X2hvFsBNXCD9Glcgd2-z0130_provenance.