Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance.
- NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_assertion description "[The overall goal of our research has been to identify the precise molecular defects in patients with ADA-deficient SCID.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance.
- NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_assertion evidence source_evidence_literature NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance.
- NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_assertion SIO_000772 2773932 NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance.
- NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_assertion wasDerivedFrom befree-2016 NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance.
- NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_assertion wasGeneratedBy ECO_0000203 NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296691.RAVjVSXNty2sw1dIi5SDnuVHpf6V5pSYnER-suoRNu92o130_provenance.