Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance.
- NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_assertion description "[Chd7(COA1/+) mice phenocopied human CHARGE syndrome and displayed developmental defects in the telencephalic midline, including dilated third and lateral ventricles, reduced cerebral cortex, and corpus callosum crossing failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance.
- NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_assertion evidence source_evidence_literature NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance.
- NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_assertion SIO_000772 22658483 NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance.
- NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_assertion wasDerivedFrom befree-2016 NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance.
- NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_assertion wasGeneratedBy ECO_0000203 NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance.
- befree-2016 importedOn "2016-02-19" NP986575.RAQKywSkCF14LkDjfzU1ug9k2IRVA5Nbvz56-TrgWL81E130_provenance.