Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance.
- NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_assertion wasGeneratedBy ECO_0000218 NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance.
- NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_assertion wasDerivedFrom ctd_human-20150221 NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance.
- NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_assertion SIO_000772 17704776 NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance.
- NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_assertion evidence source_evidence_curated NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance.
- NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_assertion description "[Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_provenance.