Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance.
- NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_assertion description "[The Val81 missense mutation of the melanocortin 3 receptor gene, but not the 1908c/T nucleotide polymorphism in lamin A/C gene, is associated with hyperleptinemia and hyperinsulinemia in obese Greek caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance.
- NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_assertion evidence source_evidence_literature NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance.
- NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_assertion SIO_000772 15636422 NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance.
- NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_assertion wasDerivedFrom gad-20150221 NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance.
- NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_assertion wasGeneratedBy ECO_0000203 NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance.
- gad-20150221 importedOn "2015-02-21" NP68944.RAIljIxmvMEUECrPXwRi07clVlC72XTe15xC3vNKS0a9Q130_provenance.