Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion> ?p ?o ?g. }
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- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion type Assertion NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_head.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_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." NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion evidence source_evidence_literature NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion SIO_000772 12112878 NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion wasDerivedFrom befree-20150227 NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion wasGeneratedBy ECO_0000203 NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.