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- source_evidence_literature type ECO_0000212 NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_provenance.
- NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_assertion description "[The OAT or AZOO patients with Sertoli cell only syndrome (SCO) had mutations in the CFTR gene with similar frequencies to that in the general Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_provenance.
- NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_assertion evidence source_evidence_literature NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_provenance.
- NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_assertion SIO_000772 16572913 NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_provenance.
- NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_assertion wasDerivedFrom befree-20140225 NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_provenance.
- NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_assertion wasGeneratedBy ECO_0000203 NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP776243.RA2WMWseCHM-M4VBYCc3l9kO8f8icaHFRuO1P-3xI7pbg130_provenance.