Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance.
- NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_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." NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance.
- NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_assertion evidence source_evidence_literature NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance.
- NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_assertion SIO_000772 24018267 NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance.
- NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_assertion wasDerivedFrom befree-20150227 NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance.
- NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_assertion wasGeneratedBy ECO_0000203 NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP433988.RAwsWRPKqkTbNjy_UcSmCNyufttXg7AEmfo7DzSd8-bwQ130_provenance.