Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_assertion> ?p ?o ?g. }
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- NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_assertion type Assertion NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_head.
- NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_assertion wasGeneratedBy ECO_0000203 NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_provenance.
- NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_assertion wasDerivedFrom befree-20140225 NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_provenance.
- NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_assertion SIO_000772 17704776 NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_provenance.
- NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_assertion evidence source_evidence_literature NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_provenance.
- NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_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." NP638273.RAWO-kmC96vIyGluwYLATueuA98oQjUEewZygfR5vaij8130_provenance.