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- NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_assertion type Assertion NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_head.
- NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_assertion wasGeneratedBy ECO_0000203 NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance.
- NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_assertion wasDerivedFrom befree-2016 NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance.
- NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_assertion SIO_000772 20560207 NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance.
- NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_assertion evidence source_evidence_literature NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance.
- NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_assertion description "[Identification of a Kir3.4 mutation in congenital long QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance.