Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance.
- NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_assertion description "[Necdin deletion is associated with Prader-Willi syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance.
- NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_assertion evidence source_evidence_literature NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance.
- NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_assertion SIO_000772 21150695 NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance.
- NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_assertion wasDerivedFrom befree-20150227 NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance.
- NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_assertion wasGeneratedBy ECO_0000203 NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP585836.RA91iUavL0VBSs3HdwcCJFTmegUSgVmRrOG-UkKyXHGLE130_provenance.