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- source_evidence_literature type ECO_0000212 NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_provenance.
- NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_assertion description "[Sequence alterations in CACNA1F lead to the incomplete type of CSNB (CSNB2), which can be distinguished by standard electroretinography (ERG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_provenance.
- NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_assertion evidence source_evidence_literature NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_provenance.
- NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_assertion SIO_000772 16960802 NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_provenance.
- NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_assertion wasDerivedFrom befree-2016 NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_provenance.
- NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_assertion wasGeneratedBy ECO_0000203 NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_provenance.
- befree-2016 importedOn "2016-02-19" NP568396.RAMbFOK0bt85ttq4LBGTzR-hj557LfMggba1joBpLgijU130_provenance.