Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance.
- NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_assertion wasGeneratedBy ECO_0000203 NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance.
- NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_assertion wasDerivedFrom befree-20140225 NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance.
- NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_assertion SIO_000772 18162506 NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance.
- NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_assertion evidence source_evidence_literature NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance.
- NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_assertion description "[We conclude that 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." NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_provenance.