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- source_evidence_literature type ECO_0000212 NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_provenance.
- NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_assertion description "[For the first time, we associate the RFC1 80G>A and NNMT IVS -151C>T variants to an increased ALL susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_provenance.
- NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_assertion evidence source_evidence_literature NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_provenance.
- NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_assertion SIO_000772 19020309 NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_provenance.
- NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_assertion wasDerivedFrom befree-2016 NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_provenance.
- NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_assertion wasGeneratedBy ECO_0000203 NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_provenance.
- befree-2016 importedOn "2016-02-19" NP704669.RAD-n3dDJb3Rbbn6LhH-mBfGOkd4k8h6V7csYY2wlvW1c130_provenance.