Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_assertion> ?p ?o ?g. }
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- NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_assertion type Assertion NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_head.
- NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_assertion wasGeneratedBy ECO_0000218 NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_provenance.
- NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_assertion wasDerivedFrom uniprot-20130724 NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_provenance.
- NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_assertion SIO_000772 12621127 NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_provenance.
- NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_assertion evidence source_evidence_curated NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_provenance.
- NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_assertion description "[Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3417.RAWnQxsizVlqzwbx9NVtWot6wY-UBKH1_E2wOyaKF6mSY130_provenance.