Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_assertion> ?p ?o ?g. }
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- NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_assertion type Assertion NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_head.
- NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_assertion wasGeneratedBy ECO_0000203 NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_provenance.
- NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_assertion wasDerivedFrom befree-2016 NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_provenance.
- NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_assertion SIO_000772 12475673 NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_provenance.
- NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_assertion evidence source_evidence_literature NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_provenance.
- NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_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." NP377304.RACFXnEYWvQegRiAJ0LdSCup_jI0TwI0pK1RnVvh0Oiyc130_provenance.