Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance.
- NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_assertion description "[Recurrent deletions of 5q in myeloid malignancies encompass two separate regions: deletion of 5q33, which is associated with the 5q? syndrome and haploinsufficiency of RPS14, and deletion of a more proximal locus at 5q31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance.
- NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_assertion evidence source_evidence_literature NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance.
- NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_assertion SIO_000772 21536236 NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance.
- NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_assertion wasDerivedFrom befree-2016 NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance.
- NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_assertion wasGeneratedBy ECO_0000203 NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance.
- befree-2016 importedOn "2016-02-19" NP891035.RAmDC3lQHPFb-PQeb4MsLPq_hv52oGJpxsCSXz2rTf8Bc130_provenance.