Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion evidence source_evidence_literature NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion SIO_000772 18807109 NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion wasDerivedFrom befree-2016 NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion wasGeneratedBy ECO_0000203 NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- befree-2016 importedOn "2016-02-19" NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.