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- source_evidence_literature type ECO_0000212 NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_provenance.
- NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_assertion description "[Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_provenance.
- NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_assertion evidence source_evidence_literature NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_provenance.
- NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_assertion SIO_000772 18752142 NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_provenance.
- NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_assertion wasDerivedFrom gad-20150221 NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_provenance.
- NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_assertion wasGeneratedBy ECO_0000203 NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP129135.RA3Jj8ccmX3bVxQ3m7KnkGkZT5A_iKHm9ARD5-Hr74aTY130_provenance.