Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance.
- NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_assertion description "[Bioinformatic searches were performed in the Single-nucleotide polymorphism database (build 132) and in the National Heart, Lung, and Blood Institute Grand Opportunity Exome Sequencing Project (ESP) for both previously published variant-BrS associations and newly uncovered variations within the noted genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance.
- NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_assertion evidence source_evidence_literature NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance.
- NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_assertion SIO_000772 22284586 NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance.
- NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_assertion wasDerivedFrom befree-20140225 NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance.
- NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_assertion wasGeneratedBy ECO_0000203 NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP332825.RAejy_9SuPJc8atkz1JJQghA51ehvoRBg1AyKwiHL0Rn0130_provenance.