Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance.
- NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_assertion description "[Significantly more -7/del(7q) (P = 0.004) and -5/del(5q) (P = 0.03) were found in AML/MDS with a higher incidence of dup1q (P = 0.01) in MF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance.
- NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_assertion evidence source_evidence_literature NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance.
- NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_assertion SIO_000772 20629097 NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance.
- NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_assertion wasDerivedFrom befree-20150227 NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance.
- NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_assertion wasGeneratedBy ECO_0000203 NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978386.RAp3-sHBal-lMp_isVIMTSHz74GMUZKrWEanUvwN1G_xY130_provenance.