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- NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_assertion type Assertion NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_head.
- NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_assertion wasGeneratedBy ECO_0000203 NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_provenance.
- NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_assertion wasDerivedFrom befree-2016 NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_provenance.
- NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_assertion SIO_000772 21222060 NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_provenance.
- NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_assertion evidence source_evidence_literature NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_provenance.
- NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_assertion description "[CFTR and/or SPINK1 gene mutations associate with IP (idiopathic CP and IRAP) independently of the presence of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864479.RAYr-9YHd6kVm0yfeb92byNn8R7npuy6RDsLebsc1enWU130_provenance.