Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.
- NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.
- NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_assertion evidence source_evidence_literature NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.
- NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_assertion SIO_000772 17262171 NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.
- NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_assertion wasDerivedFrom befree-20150227 NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.
- NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_assertion wasGeneratedBy ECO_0000203 NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP673545.RAbU5gqd6avn_DVy-Z-dRfllqpJxQvnyqAsYWJAzr_IyA130_provenance.