Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_assertion type Assertion NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_head.
- NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_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." NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance.
- NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_assertion evidence source_evidence_literature NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance.
- NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_assertion SIO_000772 18288099 NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance.
- NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_assertion wasDerivedFrom befree-2016 NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance.
- NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_assertion wasGeneratedBy ECO_0000203 NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance.