Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance.
- NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_assertion description "[Neuregulin 1-induced AKT and ERK phosphorylation in patients with fragile X syndrome (FXS) and intellectual disability associated with obstetric complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance.
- NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_assertion evidence source_evidence_literature NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance.
- NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_assertion SIO_000772 24563264 NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance.
- NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_assertion wasDerivedFrom befree-2016 NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance.
- NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_assertion wasGeneratedBy ECO_0000203 NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1157539.RAmgurMrSwyv8SXYreGUZk_BTluKy2olFvVlOYcuR-Xbg130_provenance.