Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance.
- NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_assertion wasGeneratedBy ECO_0000203 NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance.
- NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_assertion wasDerivedFrom gad-20150221 NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance.
- NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_assertion SIO_000772 18162506 NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance.
- NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_assertion evidence source_evidence_literature NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance.
- NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_assertion description "[INS mutations are the second most common cause of PND and a rare cause of MODY.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116912.RA4b6EhCIbX82Qmp6eiM8dxDOtZr55m8wBZkC9tt-zrpo130_provenance.