Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion evidence source_evidence_literature NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion SIO_000772 7650604 NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion wasDerivedFrom befree-20140225 NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion wasGeneratedBy ECO_0000203 NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- befree-20140225 importedOn "2014-02-25" NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.