Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_assertion> ?p ?o ?g. }
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- NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_assertion type Assertion NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_head.
- NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_assertion description "[Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_provenance.
- NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_assertion evidence source_evidence_curated NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_provenance.
- NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_assertion SIO_000772 22560297 NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_provenance.
- NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_assertion wasDerivedFrom uniprot-20130724 NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_provenance.
- NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_assertion wasGeneratedBy ECO_0000218 NP4500.RAFPs2WjYPbZ1cQ8xLZNG3ISAKW41RSoOd_VeIfjCSRH8130_provenance.