Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance.
- NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_assertion description "[Dominant mutations in the skeletal muscle ryanodine receptor (RYR1) gene are well-recognized causes of both malignant hyperthermia susceptibility (MHS) and central core disease (CCD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance.
- NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_assertion evidence source_evidence_literature NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance.
- NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_assertion SIO_000772 17483490 NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance.
- NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_assertion wasDerivedFrom befree-2016 NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance.
- NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_assertion wasGeneratedBy ECO_0000203 NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance.
- befree-2016 importedOn "2016-02-19" NP608536.RAholocBGFtpGFidsdEe_KeTUg6aiG3SqMCjQNSolWwbY130_provenance.