Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance.
- NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_assertion description "[PRSS1: IVS 2 +56_60 del CCCAG is a noval mutant which may contribute to AIP pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance.
- NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_assertion evidence source_evidence_literature NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance.
- NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_assertion SIO_000772 24236450 NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance.
- NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_assertion wasDerivedFrom befree-2016 NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance.
- NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_assertion wasGeneratedBy ECO_0000203 NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1128284.RA70VP0K9lz-mWk7XQUrK5LQR6FqpNotyl0vJmC-qhmsU130_provenance.