Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_assertion> ?p ?o ?g. }
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- NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_assertion type Assertion NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_head.
- NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_assertion wasGeneratedBy ECO_0000218 NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_provenance.
- NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_assertion wasDerivedFrom ctd_human-20130708 NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_provenance.
- NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_assertion SIO_000772 17704776 NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_provenance.
- NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_assertion evidence source_evidence_curated NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_provenance.
- NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_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." NP30841.RAKPmlQhG472AODIxqow44tqw4nGjpLltlQxAq1SJJAho130_provenance.