Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance.
- NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_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." NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance.
- NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_assertion evidence source_evidence_literature NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance.
- NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_assertion SIO_000772 20629097 NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance.
- NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_assertion wasDerivedFrom befree-20150227 NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance.
- NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_assertion wasGeneratedBy ECO_0000203 NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP913878.RAunnoLGgfOu3io5BFHx1lsrlzL7mJeLvi_tSPht5COSE130_provenance.