Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance.
- NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_assertion description "[The NKX-3.1 homeobox gene maps to human chromosome 8p21, a region that undergoes frequent loss of heterozygosity in prostate tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance.
- NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_assertion evidence source_evidence_literature NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance.
- NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_assertion SIO_000772 11809674 NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance.
- NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_assertion wasDerivedFrom befree-20140225 NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance.
- NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_assertion wasGeneratedBy ECO_0000203 NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP764862.RAtQ_OufjmnWsbZ6jP1VXVvESTKjSYEFPNuOYnGJcbemw130_provenance.