Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance.
- NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_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." NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance.
- NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_assertion evidence source_evidence_literature NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance.
- NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_assertion SIO_000772 23361065 NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance.
- NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_assertion wasDerivedFrom befree-20140225 NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance.
- NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_assertion wasGeneratedBy ECO_0000203 NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance.
- befree-20140225 importedOn "2014-02-25" NP239306.RAxFfD33btN52QO4Ha2Cv0boK64skRQoJr1QoEixrLh94130_provenance.