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- source_evidence_literature type ECO_0000212 NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_provenance.
- NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_assertion description "[Mutations have been identified in MH-susceptible (MHS) individuals in two key proteins of excitation-contraction (EC) coupling, the Ca2+ release channel of the SR, ryanodine receptor type 1 (RyR1) and the alpha1-subunit of the dihydropyridine receptor (DHPR, L-type Ca2+ channel).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_provenance.
- NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_assertion evidence source_evidence_literature NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_provenance.
- NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_assertion SIO_000772 11412150 NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_provenance.
- NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_assertion wasDerivedFrom befree-20140225 NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_provenance.
- NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_assertion wasGeneratedBy ECO_0000203 NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP822349.RAGYliXzpCvhYnBzrqUwOxPskm9rkq-EBwaSU693n9HYc130_provenance.