Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance.
- NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_assertion description "[germline mutations with familial hyperparathyroidism associated with 80% recurrence/persistence rate, increasingly difficult re-operations and risk of parathyroid carcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance.
- NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_assertion evidence source_evidence_literature NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance.
- NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_assertion SIO_000772 18436011 NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance.
- NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_assertion wasDerivedFrom lhgdn-20090331 NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance.
- NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_assertion wasGeneratedBy ECO_0000203 NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP237114.RA7J721V2NIO32tbQ1vCV6WhPkufPGR--JJ6_haZMHUT0130_provenance.