Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance.
- NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_assertion description "[Therefore, a comprehensive genome-wide analysis of patients with AML or MDS with complex karyotypes has led to a better characterization of chromosomal aberrations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance.
- NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_assertion evidence source_evidence_literature NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance.
- NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_assertion SIO_000772 16142824 NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance.
- NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_assertion wasDerivedFrom befree-20150227 NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance.
- NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_assertion wasGeneratedBy ECO_0000203 NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance.
- befree-20150227 importedOn "2015-02-27" NP873092.RA3RVQDQGSrX_fs_HbVi2ytF7wO9a1-xnYdeRwKVA7Tro130_provenance.