Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance.
- NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_assertion description "[We studied 29 patients with FRDA (10 men, mean age 31+/-9 years) who were homozygous for the GAA expansion in the FRDA gene and were without cardiac symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance.
- NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_assertion evidence source_evidence_literature NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance.
- NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_assertion SIO_000772 10982543 NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance.
- NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_assertion wasDerivedFrom befree-2016 NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance.
- NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_assertion wasGeneratedBy ECO_0000203 NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance.
- befree-2016 importedOn "2016-02-19" NP294799.RAonAO558zpdMY52wwfWkWt-M57LnouyS-fXAlx_wWdDE130_provenance.