Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP656508.RAQe3fGGdrNsn-4LusuZxDT4YfWWx64N4FlXbuG0VBAF0130_provenance.