Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance.
- NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_assertion description "[Of these 17 patients, five patients (four with BCC and one with SCC) (29%) showed loss of one of the c-Ha-ras alleles in their tumor DNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance.
- NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_assertion evidence source_evidence_literature NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance.
- NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_assertion SIO_000772 2690853 NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance.
- NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_assertion wasDerivedFrom befree-20150227 NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance.
- NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_assertion wasGeneratedBy ECO_0000203 NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP465378.RAQkH8_Q6YFxZ2_ap_O7_CVirRjgEgVOgSPQtn83d4SOg130_provenance.