Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_assertion> ?p ?o ?g. }
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- NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_assertion type Assertion NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_head.
- NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_assertion wasGeneratedBy ECO_0000203 NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_provenance.
- NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_assertion wasDerivedFrom befree-2016 NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_provenance.
- NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_assertion SIO_000772 15761194 NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_provenance.
- NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_assertion evidence source_evidence_literature NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_provenance.
- NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485080.RAUfEXm9XN4VDqr2Rh0Ydh6NKqZQ7Q4P8We_lfAAm57Qk130_provenance.