Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_assertion> ?p ?o ?g. }
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- NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_assertion type Assertion NP31110.RAFjc1u9vsq0OFnVRHcF8EOYqQyic0d-Lxrp2Wo1VozaU130_head.
- 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.