Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_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." NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion evidence source_evidence_literature NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion SIO_000772 12112878 NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion wasDerivedFrom befree-20150227 NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_assertion wasGeneratedBy ECO_0000203 NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP787165.RAEEmsWtPQTcRaNoplEM-leuew7D4uQJykYxZKjyixX5s130_provenance.