Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance.
- NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_assertion wasGeneratedBy ECO_0000203 NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance.
- NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_assertion wasDerivedFrom befree-20140225 NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance.
- NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_assertion SIO_000772 19407509 NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance.
- NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_assertion evidence source_evidence_literature NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance.
- NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_assertion description "[The rarity of MEN1 mutations in some MEN1-like states aids the identification of other mutated genes, such as AIP, HRPT2 and p27(Kip1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP394841.RAexwnFaZP0Wf7hpk9veQJgQy2TEKLNCPb8Wwa4El6TU8130_provenance.