Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance.
- NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_assertion description "[Functional analysis using neuroblastoma cell lines expressing mutant TrkC demonstrated that one of the mutations (c.278C>T, p.T93M) significantly reduced autophosphorylation of TrkC in response to ligand binding, subsequently decreasing phosphorylation of downstream target proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance.
- NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_assertion evidence source_evidence_literature NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance.
- NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_assertion SIO_000772 25196463 NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance.
- NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_assertion wasDerivedFrom befree-2016 NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance.
- NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_assertion wasGeneratedBy ECO_0000203 NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1217758.RAnhhpTh-yuTq4SK8wCOLje2hFfUAciJNNCNBRM1xyJm8130_provenance.