Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance.
- NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_assertion description "[These findings illustrate the high prevalence of MetS in SGA-treated children and suggest metabolic alterations associated with the MTHFR C677T variant may have a role in the development of MetS features in SGA-treated children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance.
- NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_assertion evidence source_evidence_literature NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance.
- NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_assertion SIO_000772 22832733 NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance.
- NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_assertion wasDerivedFrom befree-20140225 NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance.
- NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_assertion wasGeneratedBy ECO_0000203 NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP400649.RA33EaG3XTU7r9_i_XSiiahwCvBfjccWv8ukFH64KHi7c130_provenance.