Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.
- NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_assertion description "[The Ala4894Thr RyR1 variant was found in a Japanese patient with susceptibility to MH, and the Ala4894Pro variant in a rare case of myopathy: congenital neuromuscular disease with uniform type 1 fiber (CNMDU1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.
- NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_assertion evidence source_evidence_literature NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.
- NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_assertion SIO_000772 21926372 NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.
- NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_assertion wasDerivedFrom befree-20140225 NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.
- NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_assertion wasGeneratedBy ECO_0000203 NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.
- befree-20140225 importedOn "2014-02-25" NP550607.RAohDwuoUVrT3tjVgy0KercJkFcl98OJYuZLCS_SpZb00130_provenance.