Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_assertion> ?p ?o ?g. }
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- NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_assertion type Assertion NP271716.RAadT_hqmpR3p-yOl1oPaD0dFNTh7vuN5IN81IDgZigOc130_head.
- 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.