Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance.
- NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_assertion description "[Genotype-phenotype associations for ARX gene duplication in X-linked mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance.
- NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_assertion evidence source_evidence_literature NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance.
- NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_assertion SIO_000772 17082467 NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance.
- NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_assertion wasDerivedFrom befree-2016 NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance.
- NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_assertion wasGeneratedBy ECO_0000203 NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance.
- befree-2016 importedOn "2016-02-19" NP577525.RAeeENrZ_hFTc4eHnfY2eREAOCfLIYlD2IO1hn_kH7bPg130_provenance.