Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance.
- NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_assertion description "[We studied the PRRX1 gene in a non-consanguineous Indonesian female infant who was diagnosed prenatally with severe retrognathia (bilateral Pruzansky type III).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance.
- NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_assertion evidence source_evidence_curated NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance.
- NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_assertion SIO_000772 23444262 NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance.
- NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_assertion wasDerivedFrom ctd_human-20150221 NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance.
- NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_assertion wasGeneratedBy ECO_0000218 NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP27299.RAgNBIQ0B7m8N0Lm7mFgrcKgsJ5wI7RZJ08GxJ1aRglj8130_provenance.