Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance.
- NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_assertion description "[The gene RYR1, encoding the Ca2+ release channel of skeletal muscle sarcoplasmic reticulum, is responsible for about 50% of the cases of MH and some cases of CCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance.
- NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_assertion evidence source_evidence_literature NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance.
- NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_assertion SIO_000772 11216663 NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance.
- NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_assertion wasDerivedFrom befree-20140225 NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance.
- NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_assertion wasGeneratedBy ECO_0000203 NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP225969.RAqZCOkoxYv9mb_XjIhx7hC64_5pY69YSxeXxBEBFLoqY130_provenance.