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- source_evidence_literature type ECO_0000212 NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_provenance.
- NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_assertion description "[In conclusion, we found a significant association of INSL3 gene mutations in men presenting one or more signs of TDS syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_provenance.
- NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_assertion evidence source_evidence_literature NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_provenance.
- NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_assertion SIO_000772 16687567 NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_provenance.
- NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_assertion wasDerivedFrom befree-2016 NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_provenance.
- NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_assertion wasGeneratedBy ECO_0000203 NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_provenance.
- befree-2016 importedOn "2016-02-19" NP549126.RAQHwpe63odHwmqE5pWxNNp9aarK8Ix2hdrOwfaz_kr2A130_provenance.