Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_assertion> ?p ?o ?g. }
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- NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_assertion type Assertion NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_head.
- NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_assertion wasGeneratedBy ECO_0000203 NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_provenance.
- NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_assertion wasDerivedFrom lhgdn-20090331 NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_provenance.
- NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_assertion SIO_000772 15017542 NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_provenance.
- NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_assertion evidence source_evidence_literature NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_provenance.
- NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_assertion description "[insertion/deletion polymorphism may be associated with persistent pulmonary hypertension in newborns with congenital diaphragmatic hernia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210339.RAodzNYPzmgw2rwUjEMC9j7vlmlx8MYNG81PgT_cab9Qo130_provenance.