Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_assertion> ?p ?o ?g. }
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- NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_assertion type Assertion NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_head.
- NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_assertion wasGeneratedBy ECO_0000203 NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_provenance.
- NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_assertion wasDerivedFrom gad-20150221 NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_provenance.
- NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_assertion SIO_000772 18162506 NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_provenance.
- NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_assertion evidence source_evidence_literature NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_provenance.
- NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_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." NP70201.RAcu06VVhsGurmzh0o9vWrTMKIfpZeGOVtl2II1tuLHIU130_provenance.