Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion> ?p ?o ?g. }
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- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion type Assertion NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_head.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion description "[Here we show that the targeted double inactivation of Dlx5 and Dlx6 in the mouse causes in homozygous mutant animals bilateral ectrodactyly with a severe defect of the central ray of the hindlimbs, a malformation typical of SHFM1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion evidence source_evidence_literature NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion SIO_000772 12112878 NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion wasDerivedFrom befree-20150227 NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion wasGeneratedBy ECO_0000203 NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.