Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_assertion> ?p ?o ?g. }
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- NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_assertion type Assertion NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_head.
- NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_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." NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_provenance.
- NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_assertion evidence source_evidence_literature NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_provenance.
- NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_assertion SIO_000772 24018267 NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_provenance.
- NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_assertion wasDerivedFrom befree-2016 NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_provenance.
- NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_assertion wasGeneratedBy ECO_0000203 NP1108790.RA2W5fIi9whs22_KeRo-yBhUr-ciKexzmJiEgZT7kFhx4130_provenance.