Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance.
- NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_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." NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance.
- NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_assertion evidence source_evidence_literature NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance.
- NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_assertion SIO_000772 22658483 NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance.
- NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_assertion wasDerivedFrom befree-20150227 NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance.
- NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_assertion wasGeneratedBy ECO_0000203 NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP920751.RASLMn8Dxg6unuZDHuUtxjrD7w50_94uYRoGuATaTygSE130_provenance.