Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance.
- NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_assertion description "[It is of great interest that mutations were located at the same spot (exon 8) of ZFHX1B in 3 of 4 cases, probably accounting for the unique clinical features of this newly recognized form of HSCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance.
- NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_assertion evidence source_evidence_literature NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance.
- NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_assertion SIO_000772 12149685 NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance.
- NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_assertion wasDerivedFrom befree-20140225 NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance.
- NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_assertion wasGeneratedBy ECO_0000203 NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP494276.RAiWi03d9IjnTqL1-ceoqEChd0zgflkUaqVboxQT7XNjM130_provenance.