Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance.
- NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_assertion description "[We looked for mutations of the HRPT2 gene, which encodes the parafibromin protein, in sporadic parathyroid carcinoma because germ-line inactivating HRPT2 mutations have been found in a type of familial hyperparathyroidism--hyperparathyroidism-jaw tumor (HPT-JT) syndrome--that carries an increased risk of parathyroid cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance.
- NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_assertion evidence source_evidence_literature NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance.
- NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_assertion SIO_000772 14585940 NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance.
- NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_assertion wasDerivedFrom befree-20140225 NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance.
- NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_assertion wasGeneratedBy ECO_0000203 NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP524355.RAhwrXrLnXuxyxbdstjxEJO8iy666PAyHqd2JHWIB1t7U130_provenance.