Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance.
- NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_assertion description "[The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance.
- NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_assertion evidence source_evidence_literature NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance.
- NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_assertion SIO_000772 10914677 NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance.
- NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_assertion wasDerivedFrom befree-20150227 NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance.
- NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_assertion wasGeneratedBy ECO_0000203 NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP256356.RArKhU3ad49EbO1ITIPCSwTkdnsByDFoaRx01CVTrrNK8130_provenance.