Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance.
- NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_assertion description "[TP53 mutated subclones have not previously been described in myelodysplastic syndrome with isolated del(5q) and indicates a previously unknown heterogeneity of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance.
- NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_assertion evidence source_evidence_literature NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance.
- NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_assertion SIO_000772 19797731 NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance.
- NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_assertion wasDerivedFrom befree-20140225 NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance.
- NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_assertion wasGeneratedBy ECO_0000203 NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476386.RABerhrvLt08Xbd-upSQPDt0drwSpQVL6Lbc9J26dhl0w130_provenance.