Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance.
- NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_assertion description "[Consequently, genetic tests for abnormal AMPD1 expression designed to diagnose patients with metabolic myopathy, and to evaluate genetic markers for clinical outcome in heart disease should not be based solely on the detection of a single mutant allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance.
- NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_assertion evidence source_evidence_literature NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance.
- NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_assertion SIO_000772 12117480 NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance.
- NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_assertion wasDerivedFrom befree-2016 NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance.
- NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_assertion wasGeneratedBy ECO_0000203 NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance.
- befree-2016 importedOn "2016-02-19" NP361132.RAXrR8d0_B4HSSQ8LzrlJGPcTWxvdSNqYVYdcz-wS32aw130_provenance.