Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance.
- befree-2016 importedOn "2016-02-19" NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance.
- NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_assertion wasGeneratedBy ECO_0000203 NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance.
- NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_assertion wasDerivedFrom befree-2016 NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance.
- NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_assertion SIO_000772 15911703 NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance.
- NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_assertion evidence source_evidence_literature NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance.
- NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_assertion description "[The ECG features of Andersen-Tawil syndrome (ATS) patients with KCNJ2 mutations (ATS1) have not been systematically assessed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496157.RAD6n-c1lc4AfON7fW4fDDt6wZmnGKU7bVisiHDVp-Lzo130_provenance.