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- source_evidence_literature type ECO_0000212 NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_provenance.
- NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_assertion description "[Furthermore, we found evidence that coding variants in the known susceptibility gene ABCA7, as well as candidate genes DYSF and PAXIP1, confer risk for AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_provenance.
- NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_assertion evidence source_evidence_literature NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_provenance.
- NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_assertion SIO_000772 25706306 NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_provenance.
- NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_assertion wasDerivedFrom befree-2016 NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_provenance.
- NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_assertion wasGeneratedBy ECO_0000203 NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1265707.RAKw_J20cGfJ63Dhh7t5u8OLDuf66pk5BB9XLwm9TtSBI130_provenance.