Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance.
- NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_assertion wasGeneratedBy ECO_0000203 NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance.
- NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_assertion wasDerivedFrom befree-20150227 NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance.
- NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_assertion SIO_000772 22509377 NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance.
- NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_assertion evidence source_evidence_literature NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance.
- NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_assertion description "[Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598398.RAVhXi5sI099Iigv0p0OKiD8ECsKgSCj7x7iGzCCiKH0A130_provenance.