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- source_evidence_literature type ECO_0000212 NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_provenance.
- NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_assertion description "[The influence of rare genetic variation in SLC30A8 on diabetes incidence and ?-cell function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_provenance.
- NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_assertion evidence source_evidence_literature NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_provenance.
- NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_assertion SIO_000772 24471563 NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_provenance.
- NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_assertion wasDerivedFrom befree-2016 NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_provenance.
- NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_assertion wasGeneratedBy ECO_0000203 NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1149655.RANL-jgU2xnJEYWDpBw5L6-WZBIJl2MH_ZTQpatY74VrE130_provenance.