Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance.
- NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_assertion description "[DNA samples were screened for the four common Finnish founder mutations (KCNQ1 G589D and IVS7-2A-->G, HERG L552S, and R176W), which are known to account for the majority of inherited LQTS in Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance.
- NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_assertion evidence source_evidence_literature NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance.
- NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_assertion SIO_000772 17467628 NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance.
- NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_assertion wasDerivedFrom befree-20140225 NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance.
- NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_assertion wasGeneratedBy ECO_0000203 NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP709869.RA6pFCvmif8hQd6R7a-_kLE0jHyJAVPKsYzuOAt9AVpQc130_provenance.