Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance.
- NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_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." NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance.
- NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_assertion evidence source_evidence_literature NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance.
- NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_assertion SIO_000772 11216663 NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance.
- NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_assertion wasDerivedFrom befree-2016 NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance.
- NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_assertion wasGeneratedBy ECO_0000203 NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance.
- befree-2016 importedOn "2016-02-19" NP309003.RAAcWLv6JKavhvuFyz4V1GdABNIb_U7SmQaHEmaGo8z34130_provenance.