Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance.
- NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_assertion description "[The rare apolipoprotein C-II (apoC-II) mutation, apoC-IILys19-->Thr, also known as apoC-II-v, has been found previously in association with hyperlipoproteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance.
- NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_assertion evidence source_evidence_literature NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance.
- NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_assertion SIO_000772 7923858 NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance.
- NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_assertion wasDerivedFrom befree-20150227 NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance.
- NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_assertion wasGeneratedBy ECO_0000203 NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP244355.RAWora9jWqNifaxswQ5DNDf1wGzOMmRtVc45_wMXajgN8130_provenance.