Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance.
- NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_assertion description "[Our results suggest that combining genetic markers with traditional clinical risk factors has the potential to improve our ability to assess the risk of complex diseases such as T2DM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance.
- NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_assertion evidence source_evidence_literature NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance.
- NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_assertion SIO_000772 20384434 NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance.
- NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_assertion wasDerivedFrom gad-20150221 NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance.
- NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_assertion wasGeneratedBy ECO_0000203 NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP172567.RARtXTYvhRfuueXnIo-eDDHPm_dAZ6r1Bhw5iYtgULGXo130_provenance.