Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance.
- NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_assertion description "[Highly penetrant, non-synonymous, or insertion-deletion mutations in TERF1 and TERF2 were not identified and therefore are not likely to be major genetic risk factors for the development of AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance.
- NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_assertion evidence source_evidence_literature NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance.
- NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_assertion SIO_000772 16647572 NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance.
- NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_assertion wasDerivedFrom gad-20150221 NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance.
- NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_assertion wasGeneratedBy ECO_0000203 NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP86062.RAgLIMHLx24N-8fxRvXmjhJd0_TNTvYREXtTmfa-RXEH4130_provenance.