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- source_evidence_literature type ECO_0000212 NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_provenance.
- NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_assertion description "[In 5 patients with MEN 2A, gene rearrangements, such as a gross deletion, were not found in the 880 kb NruI fragment which covered the closest region to the MEN-2A locus from the RBP3 and D10S15 loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_provenance.
- NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_assertion evidence source_evidence_literature NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_provenance.
- NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_assertion SIO_000772 1982737 NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_provenance.
- NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_assertion wasDerivedFrom befree-2016 NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_provenance.
- NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_assertion wasGeneratedBy ECO_0000203 NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_provenance.
- befree-2016 importedOn "2016-02-19" NP769287.RA637XwCIM__GKr90HDTRgEt0Rmrb91qR6Q_cqzw_UcfA130_provenance.