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- source_evidence_literature type ECO_0000212 NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion description "[Heterozygous mutations in GRN are a major cause of frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP), the second most common early-onset dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion evidence source_evidence_literature NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion SIO_000772 22608501 NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion wasDerivedFrom befree-2016 NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_assertion wasGeneratedBy ECO_0000203 NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- befree-2016 importedOn "2016-02-19" NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.