Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_assertion> ?p ?o ?g. }
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- NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_assertion type Assertion NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_head.
- NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_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." NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_provenance.
- NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_assertion evidence source_evidence_literature NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_provenance.
- NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_assertion SIO_000772 12112878 NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_provenance.
- NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_assertion wasDerivedFrom befree-2016 NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_provenance.
- NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_assertion wasGeneratedBy ECO_0000203 NP360586.RAX4jjmCEH_VYzBxjMmC2TQd90TKo602I7VHQZcC3_FTs130_provenance.