Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance.
- NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_assertion description "[Patients with homozygous C4A deficiency had less proteinuria than other patients (p = 0.02) and both homozygous and heterozygous C4A-deficient patients (p = 0.05) had fewer seizures than other patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance.
- NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_assertion evidence source_evidence_literature NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance.
- NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_assertion SIO_000772 8341140 NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance.
- NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_assertion wasDerivedFrom befree-20140225 NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance.
- NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_assertion wasGeneratedBy ECO_0000203 NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP395358.RAuq3EXJTiPksYFvuwn9y7j1uMfpu-AWbzO2dnxV6atBg130_provenance.