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- source_evidence_literature type ECO_0000212 NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_provenance.
- NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_assertion description "[Biofluid studies identify about 15% of patients with FTLD due to a genetic mutation that is associated with the specific histopathologic features of TDP-43 or a tauopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_provenance.
- NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_assertion evidence source_evidence_literature NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_provenance.
- NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_assertion SIO_000772 20881489 NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_provenance.
- NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_assertion wasDerivedFrom befree-20150227 NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_provenance.
- NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_assertion wasGeneratedBy ECO_0000203 NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP872885.RAiNGHdgoXfSSh9PGTZBosXXtj5xTzC8rrvhTiEoSAg_I130_provenance.