Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance.
- NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_assertion description "[A main task for the future is to find out whether some common LSC specific markers would be identifiable in a substantial proportion of AML cases, or whether each AML case shows a unique fingerprint of markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance.
- NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_assertion evidence source_evidence_literature NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance.
- NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_assertion SIO_000772 21044004 NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance.
- NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_assertion wasDerivedFrom befree-20140225 NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance.
- NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_assertion wasGeneratedBy ECO_0000203 NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650583.RAjX7rp3R5flnJ6a0Xjgk98xKFJYNAqQoDF3AHA7N_Zmw130_provenance.