Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance.
- NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_assertion description "[The mutation causing myotonic dystrophy (DM) has recently been identified as an unstable CTG trinucleotide repeat located in the 3' untranslated region of a gene encoding for a protein with putative serine-threonine protein kinase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance.
- NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_assertion evidence source_evidence_literature NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance.
- NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_assertion SIO_000772 8499920 NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance.
- NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_assertion wasDerivedFrom befree-20150227 NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance.
- NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_assertion wasGeneratedBy ECO_0000203 NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP853006.RAEkuJA04iUbA7rT-tXR8R0UoHTFT4UuB08xlWE5f41yU130_provenance.