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- source_evidence_literature type ECO_0000212 NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_provenance.
- NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_assertion wasGeneratedBy ECO_0000203 NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_provenance.
- NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_assertion wasDerivedFrom befree-20150227 NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_provenance.
- NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_assertion SIO_000772 15072700 NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_provenance.
- NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_assertion evidence source_evidence_literature NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_provenance.
- NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_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." NP225919.RAYiAPTB1AZTqut8vwCAhnHh-SSN5fK3W66-4bEdQt48E130_provenance.