Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_assertion> ?p ?o ?g. }
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- NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_assertion type Assertion NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_head.
- NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_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." NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_provenance.
- NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_assertion evidence source_evidence_literature NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_provenance.
- NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_assertion SIO_000772 12112878 NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_provenance.
- NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_assertion wasDerivedFrom befree-2016 NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_provenance.
- NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_assertion wasGeneratedBy ECO_0000203 NP360581.RARTRqOoZzP42wkIKtxZApyg01SMWJcvns7eyqzRZ-M_c130_provenance.