Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP819777.RAYbg_vha04fNUzknkHx2iH3P4Sp_MJrVQGQWl5VdFNcQ130_provenance.
- 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.