Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance.
- NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_assertion description "[PGRN mutations were also identified in other neurodegenerative brain diseases such as amyotrophic lateral sclerosis and Alzheimer disease, though their biologic contribution to these diseases remains elusive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance.
- NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_assertion evidence source_evidence_literature NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance.
- NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_assertion SIO_000772 18838661 NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance.
- NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_assertion wasDerivedFrom befree-20140225 NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance.
- NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_assertion wasGeneratedBy ECO_0000203 NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP635926.RADH-Z1vs10p1CsU_5qqXkz8DTzU9PP9IKD1PsvBz01pA130_provenance.