Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_assertion type Assertion NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_head.
- NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_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." NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_provenance.
- NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_assertion evidence source_evidence_literature NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_provenance.
- NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_assertion SIO_000772 12112878 NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_provenance.
- NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_assertion wasDerivedFrom befree-2016 NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_provenance.
- NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_assertion wasGeneratedBy ECO_0000203 NP360582.RAx7PT9k7M4qTsvO4z9cRcvO7BJy2cBsJmSsS6SpEdYtA130_provenance.