Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.
- NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_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." NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.
- NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_assertion evidence source_evidence_literature NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.
- NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_assertion SIO_000772 12112878 NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.
- NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_assertion wasDerivedFrom befree-20140225 NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.
- NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_assertion wasGeneratedBy ECO_0000203 NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP372289.RA7bltUDILn5vSXHqss4smS3r3H2LeAEQsNKREh2zt4Hg130_provenance.