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- source_evidence_literature type ECO_0000212 NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_provenance.
- NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_assertion description "[Here we report the identification of three new CNGA3 mutations in patients with achromatopsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_provenance.
- NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_assertion evidence source_evidence_literature NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_provenance.
- NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_assertion SIO_000772 18445228 NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_provenance.
- NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_assertion wasDerivedFrom befree-2016 NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_provenance.
- NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_assertion wasGeneratedBy ECO_0000203 NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_provenance.
- befree-2016 importedOn "2016-02-19" NP668477.RAKul71Ny0SkgcpYJtc3Aahr-iPcAd5pB98o3-uxt0csY130_provenance.