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- source_evidence_literature type ECO_0000212 NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_provenance.
- NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_assertion description "[Patients with intermediate sweat chloride values and two CFTR mutations or an abnormal NPD measurement have a CF-like phenotype compatible with CFTR dysfunction and, as a group, differ phenotypically from patients with intermediate sweat chloride values in whom further CF diagnostic tests are normal as well as from CF-PS and CF-PI patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_provenance.
- NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_assertion evidence source_evidence_literature NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_provenance.
- NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_assertion SIO_000772 19318346 NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_provenance.
- NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_assertion wasDerivedFrom befree-20140225 NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_provenance.
- NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_assertion wasGeneratedBy ECO_0000203 NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477804.RAOJL1nu37eYF8bfazg9wQzu185ee_injnolR5FbAEoto130_provenance.