Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance.
- NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_assertion description "[Five de novo mutations were identified in four genes (SCNN1A, KCNJ16, KCNB2, and KCNT1) in three BrS patients (20%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance.
- NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_assertion evidence source_evidence_literature NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance.
- NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_assertion SIO_000772 25339316 NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance.
- NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_assertion wasDerivedFrom befree-2016 NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance.
- NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_assertion wasGeneratedBy ECO_0000203 NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231933.RAPHn9VVoarqKE-d_4WcDdGzBvQBEAdDc8nsf0Xd1_7Ew130_provenance.