Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance.
- NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_assertion description "[Detection of gene copy number aberrations in mantle cell lymphoma by a single quantitative multiplex PCR assay: clinicopathological relevance and prognosis value.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance.
- NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_assertion evidence source_evidence_literature NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance.
- NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_assertion SIO_000772 19594747 NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance.
- NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_assertion wasDerivedFrom gad-20150221 NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance.
- NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_assertion wasGeneratedBy ECO_0000203 NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP152519.RAUgH_PVTMVnvhlmFT0uhFqSi-XFzcOLQXXf2mhnV3POA130_provenance.