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- source_evidence_literature type ECO_0000212 NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_provenance.
- NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_assertion description "[Numerous loss-of-function mutations in the progranulin (GRN) gene cause frontotemporal lobar degeneration with ubiquitin and TAR-DNA binding protein 43-positive inclusions by reduced production and secretion of GRN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_provenance.
- NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_assertion evidence source_evidence_literature NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_provenance.
- NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_assertion SIO_000772 21289198 NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_provenance.
- NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_assertion wasDerivedFrom befree-2016 NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_provenance.
- NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_assertion wasGeneratedBy ECO_0000203 NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_provenance.
- befree-2016 importedOn "2016-02-19" NP869774.RArxhpvnI0gNgsvgt0Y99GCHc_NHJquxxg8ddBjxAnHyY130_provenance.