Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance.
- NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_assertion description "[A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance.
- NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_assertion evidence source_evidence_curated NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance.
- NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_assertion SIO_000772 19559301 NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance.
- NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_assertion wasDerivedFrom ctd_human-2016 NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance.
- NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_assertion wasGeneratedBy ECO_0000218 NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP24285.RAQ9DK_Mq7t19jBrGbtw3hS-oWMGmUoMVif7O29pEo4f0130_provenance.