Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance.
- NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_assertion description "[The myotonic disorders, including the myotonic dystrophies (myotonic dystrophy type 1, DM1; myotonic dystrophy type 2, DM2/PROMM/PDM), the muscle channelopathies or non-dystrophic myotonias (chloride, sodium, calcium and potassium channelopathies) are all characterized by myotonia and muscle weakness despite different pathophysiology involved in these disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance.
- NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_assertion evidence source_evidence_literature NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance.
- NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_assertion SIO_000772 15269662 NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance.
- NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_assertion wasDerivedFrom befree-20140225 NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance.
- NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_assertion wasGeneratedBy ECO_0000203 NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP610126.RAYnj6ECDvN_gsLEaQETCzWculWiVLl5NqW6X8dAfGP3s130_provenance.