Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance.
- NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_assertion description "[Exon scanning of all nine SMARCB1 exons in genomic DNA from our cohort of families meeting the criteria for 'definite' or 'presumptive' schwannomatosis previously revealed constitutional alterations in 13 of 19 families (68%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance.
- NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_assertion evidence source_evidence_literature NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance.
- NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_assertion SIO_000772 22949514 NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance.
- NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_assertion wasDerivedFrom befree-20140225 NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance.
- NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_assertion wasGeneratedBy ECO_0000203 NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP597162.RAMzNpT1UCSQ_zBI3cn3FWAajv1c3CG6ZCFEOktUy2DMY130_provenance.