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- source_evidence_literature type ECO_0000212 NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_provenance.
- NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_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." NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_provenance.
- NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_assertion evidence source_evidence_literature NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_provenance.
- NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_assertion SIO_000772 11890856 NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_provenance.
- NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_assertion wasDerivedFrom befree-20150227 NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_provenance.
- NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_assertion wasGeneratedBy ECO_0000203 NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP878294.RAso8x2pqHAT6eybSw5IVNgIFnoyMjRO_IwBdcTTk4Pjg130_provenance.