Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance.
- NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_assertion description "[In this study, we sequenced the TUBB2B and TUBA1A coding regions in 47 patients with a diagnosis of polymicrogyria and five with an atypical lissencephaly on neuroimaging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance.
- NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_assertion evidence source_evidence_literature NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance.
- NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_assertion SIO_000772 23361065 NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance.
- NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_assertion wasDerivedFrom befree-20150227 NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance.
- NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_assertion wasGeneratedBy ECO_0000203 NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance.
- befree-20150227 importedOn "2015-02-27" NP784114.RARwD7W8Rjz7rrDGaJmPAcXcIHj3Qezu7YPN7BJEC82ls130_provenance.