Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance.
- NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_assertion description "[The mutated alleles identified in our Japanese patients with OPMD were most likely due to duplications of (GCG)(3)GCA and (GCG)(2)(GCA)(3) but not simple expansions of the GCG repeats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance.
- NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_assertion evidence source_evidence_literature NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance.
- NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_assertion SIO_000772 11890856 NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance.
- NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_assertion wasDerivedFrom befree-2016 NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance.
- NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_assertion wasGeneratedBy ECO_0000203 NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance.
- befree-2016 importedOn "2016-02-19" NP347797.RAR8_EfdxLradkiDi81OYwMWP_zGsbRTaIv6z8tvV5PE4130_provenance.