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- source_evidence_literature type ECO_0000212 NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_provenance.
- NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_assertion description "[Therefore, as a supplement to ERG and genetic testing, we advocate the use of FAF and SD OCT in the examination of patients with CSNB2 and RP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_provenance.
- NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_assertion evidence source_evidence_literature NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_provenance.
- NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_assertion SIO_000772 21920492 NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_provenance.
- NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_assertion wasDerivedFrom befree-2016 NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_provenance.
- NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_assertion wasGeneratedBy ECO_0000203 NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_provenance.
- befree-2016 importedOn "2016-02-19" NP924104.RAUxW50ccagnAu1IYj_bUtiN5n0cqDwpDUZSajj1wuqRc130_provenance.