Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance.
- NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_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." NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance.
- NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_assertion evidence source_evidence_literature NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance.
- NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_assertion SIO_000772 15636422 NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance.
- NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_assertion wasDerivedFrom befree-20140225 NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance.
- NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_assertion wasGeneratedBy ECO_0000203 NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP189983.RADfG547oTmWknF2SY0i_c6zDMGnJXKGcOCxYeUNgig3w130_provenance.