Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_assertion> ?p ?o ?g. }
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- NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_assertion type Assertion NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_head.
- NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_assertion wasGeneratedBy ECO_0000203 NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_provenance.
- NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_assertion wasDerivedFrom befree-20140225 NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_provenance.
- NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_assertion SIO_000772 10688323 NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_provenance.
- NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_assertion evidence source_evidence_literature NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_provenance.
- NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493721.RA4aPs9xASqZY4VoM9SVsrV1UqqpVljeRaWvzi1rB5qmY130_provenance.