Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance.
- NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_assertion description "[A loss of the DNA copy number at chromosomal region 11q23-24 as detected by comparative genomic hybridization (CGH) is a marker of poor prognosis in patients with endometrial cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance.
- NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_assertion evidence source_evidence_literature NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance.
- NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_assertion SIO_000772 14533001 NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance.
- NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_assertion wasDerivedFrom befree-20140225 NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance.
- NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_assertion wasGeneratedBy ECO_0000203 NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP579101.RAyQBk9RRXmdvzBV57rIxt0YjVYWvcAL8bSD8MgUHtHbs130_provenance.