Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance.
- befree-2016 importedOn "2016-02-19" NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance.
- NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_assertion wasGeneratedBy ECO_0000203 NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance.
- NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_assertion wasDerivedFrom befree-2016 NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance.
- NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_assertion SIO_000772 20858596 NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance.
- NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_assertion evidence source_evidence_literature NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance.
- NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_assertion description "[Mutations in transcription factor FOXP2 cause difficulties mastering fluent speech (developmental verbal dyspraxia, DVD), whereas mutations of sushi-repeat protein SRPX2 lead to epilepsy of the rolandic (sylvian) speech areas, with DVD or with bilateral perisylvian polymicrogyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840821.RA3OZ41RGmgmjaI8VQdYByRn4I3A3oIf6BpK5OYMIm3Nw130_provenance.