Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance.
- NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_assertion wasGeneratedBy ECO_0000203 NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance.
- NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_assertion wasDerivedFrom befree-20140225 NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance.
- NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_assertion SIO_000772 20833339 NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance.
- NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_assertion evidence source_evidence_literature NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance.
- NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_assertion description "[We now recognise that somatic mutations in MEN1 and HRPT2 tumour suppressor genes are frequent events in sporadic parathyroid adenomas and carcinomas, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP514486.RAMS4F-xBKFVV2kd9Rhezikz_zb4Gr0yKHGtWiBsW9FJ4130_provenance.