Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance.
- NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_assertion wasGeneratedBy ECO_0000203 NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance.
- NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_assertion wasDerivedFrom befree-2016 NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance.
- NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_assertion SIO_000772 9576197 NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance.
- NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_assertion evidence source_evidence_literature NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance.
- NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_assertion description "[Trisomy 12 cases demonstrated a significant higher expression of CD11a (P<0.0001) and CD20 (P<0.0006) when compared to cases with the equivalent morphology and immunophenotype, but without the chromosomal abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1394565.RAiDGItpTXzjtK-kahKctMeFxH1mv91ssYGYOJya6UoR0130_provenance.