Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.
- NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_assertion wasGeneratedBy ECO_0000203 NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.
- NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_assertion wasDerivedFrom befree-20150227 NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.
- NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_assertion SIO_000772 10898405 NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.
- NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_assertion evidence source_evidence_literature NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.
- NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_assertion description "[The much rarer Jervell-Lange-Nielsen syndrome (with marked QT prolongation and sensorineural deafness) arises when a child inherits mutant KVLQT1 or minK alleles from both parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523139.RAqQUzLERpkC6hfjfHgICBUF4AR559G5mNDt8NyL5q64k130_provenance.