Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_assertion> ?p ?o ?g. }
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- NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_assertion type Assertion NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_head.
- NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_assertion description "[Because genetic variants of the hMT2 receptor are considered to be risk factors in the development of type 2 diabetes, our results are potentially significant in explaining and preventing the pathogenesis of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance.
- NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_assertion evidence source_evidence_literature NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance.
- NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_assertion SIO_000772 21585522 NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance.
- NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_assertion wasDerivedFrom befree-20150227 NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance.
- NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_assertion wasGeneratedBy ECO_0000203 NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance.