Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance.
- NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_assertion description "[Therefore, ZNF127 and ZNF127AS are novel imprinted genes that may be associated with some of the clinical features of the polygenic Prader-Willi syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance.
- NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_assertion evidence source_evidence_literature NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance.
- NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_assertion SIO_000772 10196367 NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance.
- NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_assertion wasDerivedFrom befree-20150227 NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance.
- NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_assertion wasGeneratedBy ECO_0000203 NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP836553.RAy_1eT0FAteNBGG5OVg9x1R7UZQ0GzDad4vU724FAEvQ130_provenance.