Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP465629.RAqRxj48oaoEPLRvWpA52mHIkb705K1pFBw2DuixJXN_k130_provenance.