Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance.
- NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_assertion description "[The commonly deleted region of the 5q- syndrome extends between the genes SH3TC2 (proximal boundary) and GLRA1 (distal boundary) and measures 2.9 Mb.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance.
- NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_assertion evidence source_evidence_literature NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance.
- NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_assertion SIO_000772 18508791 NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance.
- NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_assertion wasDerivedFrom befree-20150227 NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance.
- NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_assertion wasGeneratedBy ECO_0000203 NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP428872.RArToMdJTY5JSUGsWcNTdSIf1QpmXOxUacegVsXBznVcA130_provenance.