Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance.
- NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_assertion description "[The discovery that mutations in the gene encoding for progranulin (GRN) cause frontotemporal lobar degeneration (FTLD) and other neurodegenerative diseases leading to dementia has brought renewed interest in progranulin and its functions in the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance.
- NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_assertion evidence source_evidence_literature NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance.
- NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_assertion SIO_000772 24018267 NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance.
- NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_assertion wasDerivedFrom befree-2016 NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance.
- NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_assertion wasGeneratedBy ECO_0000203 NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1108787.RAlBU427nveQg8c00SCZFF7Cb8PhaQAxsuTv32ChcCw3s130_provenance.