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- source_evidence_literature type ECO_0000212 NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_provenance.
- NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_assertion wasGeneratedBy ECO_0000203 NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_provenance.
- NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_assertion wasDerivedFrom befree-20150227 NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_provenance.
- NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_assertion SIO_000772 20829227 NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_provenance.
- NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_assertion evidence source_evidence_literature NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_provenance.
- NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_assertion description "[These new findings demonstrate that the spectrum of TUBB3-related phenotype is broader than previously described and includes malformations of cortical development (MCD) associated with neuronal migration and differentiation defects, axonal guidance and tract organization impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831561.RAAuzaHEqDSViwaaVEMn-Qj_i3ZECitOxOx2nrgACn2tw130_provenance.