Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance.
- NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_assertion description "[Rare individuals with PWS who carry atypical microdeletions on chromosome 15q have narrowed the critical region for this disorder to a 108 kb region that includes the SNORD116 snoRNA cluster and the Imprinted in Prader-Willi (IPW) non-coding RNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance.
- NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_assertion evidence source_evidence_literature NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance.
- NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_assertion SIO_000772 24363065 NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance.
- NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_assertion wasDerivedFrom befree-20150227 NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance.
- NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_assertion wasGeneratedBy ECO_0000203 NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP959286.RAup98nOANE1_phjZOlOvFvI7N81Ae-ZDzz2vR_Bijmk4130_provenance.