Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_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." NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion evidence source_evidence_literature NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion SIO_000772 12112878 NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion wasDerivedFrom befree-20150227 NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_assertion wasGeneratedBy ECO_0000203 NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP355012.RANAZA_u-_TS--eH3zoVvLcPO7fmDbNMRqVb3P0wz1ClQ130_provenance.