Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.
- NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_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." NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.
- NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_assertion evidence source_evidence_literature NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.
- NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_assertion SIO_000772 12112878 NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.
- NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_assertion wasDerivedFrom befree-2016 NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.
- NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_assertion wasGeneratedBy ECO_0000203 NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.
- befree-2016 importedOn "2016-02-19" NP360587.RAzYzrQ74tXHNClkLXG8Rw7dV4Y8jMWE4JxE5KQC3nQN8130_provenance.