Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_assertion> ?p ?o ?g. }
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- NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_assertion type Assertion NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_head.
- NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_assertion description "[Coinheritance of p.R75Q or CF causing CFTR variants with SPINK1 variants significantly increases the risk of ICP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_provenance.
- NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_assertion evidence source_evidence_literature NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_provenance.
- NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_assertion SIO_000772 20977904 NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_provenance.
- NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_assertion wasDerivedFrom befree-20150227 NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_provenance.
- NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_assertion wasGeneratedBy ECO_0000203 NP311482.RAXd9F4zUfaDLZllDUvpf9VGLGGj8XqDmmqz61kolLmjc130_provenance.