Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance.
- NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_assertion description "[Notably, the disease mutations promote excess incorporation of hnRNPA2 and hnRNPA1 into stress granules and drive the formation of cytoplasmic inclusions in animal models that recapitulate the human pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance.
- NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_assertion evidence source_evidence_literature NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance.
- NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_assertion SIO_000772 23455423 NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance.
- NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_assertion wasDerivedFrom befree-20150227 NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance.
- NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_assertion wasGeneratedBy ECO_0000203 NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP461764.RAlNbcFn8XvGNhjnrs4rQX2q7KHaewiqUK1M4Jo3UBMd0130_provenance.