Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance.
- befree-2016 importedOn "2016-02-19" NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance.
- NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_assertion wasGeneratedBy ECO_0000203 NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance.
- NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_assertion wasDerivedFrom befree-2016 NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance.
- NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_assertion SIO_000772 15072700 NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance.
- NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_assertion evidence source_evidence_literature NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance.
- NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_assertion description "[The clinical features of TPP resemble familial hypokalemic periodic paralysis (hypoKPP), which has been linked to two mutations in the gene encoding the skeletal muscle calcium channel alpha-1 subunit (CACN1AS; Arg528His and Arg1239His) and to the sodium channel alpha-subunit (SCN4A; Arg672His).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439069.RAsJuwlNsC4TLlSumCJhASwnUSvIUOv3rvY036As9_etM130_provenance.