Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.
- NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_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." NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.
- NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_assertion evidence source_evidence_literature NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.
- NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_assertion SIO_000772 22608501 NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.
- NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_assertion wasDerivedFrom befree-20150227 NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.
- NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_assertion wasGeneratedBy ECO_0000203 NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.