Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_assertion> ?p ?o ?g. }
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- NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_assertion type Assertion NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_head.
- NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_assertion wasGeneratedBy ECO_0000203 NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_provenance.
- NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_assertion wasDerivedFrom befree-20150227 NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_provenance.
- NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_assertion SIO_000772 12475673 NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_provenance.
- NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_assertion evidence source_evidence_literature NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_provenance.
- NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_assertion description "[CUAVD is important because of its association with renal anomalies and cystic fibrosis transmembrane conductance regulator gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311423.RAgO56zWaK9ydOlvH6da_S4fnhT9dhCQCoJhxPMZRWAvU130_provenance.