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- source_evidence_literature type ECO_0000212 NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_provenance.
- befree-2016 importedOn "2016-02-19" NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_provenance.
- NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_assertion wasGeneratedBy ECO_0000203 NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_provenance.
- NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_assertion wasDerivedFrom befree-2016 NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_provenance.
- NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_assertion SIO_000772 21616505 NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_provenance.
- NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_assertion evidence source_evidence_literature NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_provenance.
- NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_assertion description "[NOTCH3 gene mutations in subjects clinically suspected of CADASIL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897053.RADOFdp5veW1c5mgF8qN0WnxvAviABMExv2fYB-VXGb1o130_provenance.