Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_assertion> ?p ?o ?g. }
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- NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_assertion type Assertion NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_head.
- NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_assertion description "[Many mutations in the Human Ether-�-go-go-Related Gene (HERG) cause type 2 congenital long QT syndrome (LQT2) by disrupting trafficking of the HERG-encoded potassium channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_provenance.
- NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_assertion evidence source_evidence_literature NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_provenance.
- NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_assertion SIO_000772 12270925 NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_provenance.
- NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_assertion wasDerivedFrom befree-20140225 NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_provenance.
- NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_assertion wasGeneratedBy ECO_0000203 NP184968.RAR9QER_Zf669INvqT5yGr-prEEqBJdSAYpl38-AXKdLs130_provenance.