Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_assertion> ?p ?o ?g. }
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- NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_assertion type Assertion NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_head.
- NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_assertion description "[We sequenced the entire coding region and splice sites of CDKN1B in 50 parathyroid tumors from 35 patients to see if inactivating mutations could cause monoclonal tumorigenesis in refractory secondary/tertiary hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_provenance.
- NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_assertion evidence source_evidence_literature NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_provenance.
- NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_assertion SIO_000772 18288099 NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_provenance.
- NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_assertion wasDerivedFrom befree-20150227 NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_provenance.
- NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_assertion wasGeneratedBy ECO_0000203 NP303530.RAYbAYSk3vgxW3RKMXMMgkDhvaRVHL9-eURYLKy9GGt_E130_provenance.