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- source_evidence_literature type ECO_0000212 NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_provenance.
- NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_assertion description "[Type 1 DM (DM1) is caused by a (CTG)(n) expansion in the 3' untranslated region of DMPK in 19q13.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_provenance.
- NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_assertion evidence source_evidence_literature NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_provenance.
- NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_assertion SIO_000772 12970845 NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_provenance.
- NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_assertion wasDerivedFrom befree-2016 NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_provenance.
- NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_assertion wasGeneratedBy ECO_0000203 NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_provenance.
- befree-2016 importedOn "2016-02-19" NP408694.RAcfgaF-8HUFPAomxVzxARwLd_O2kG2O3wqh2ELjkwOOY130_provenance.