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- source_evidence_literature type ECO_0000212 NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_provenance.
- NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_assertion description "[Further evaluation in a larger sample of patients is needed in order to better define the prognostic and clinical value, if any, of MTHFR 1298 polymorphisms and CDKN2A and Snk/Plk2 methylation in the pathogenesis of MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_provenance.
- NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_assertion evidence source_evidence_literature NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_provenance.
- NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_assertion SIO_000772 21067440 NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_provenance.
- NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_assertion wasDerivedFrom befree-2016 NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_provenance.
- NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_assertion wasGeneratedBy ECO_0000203 NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_provenance.
- befree-2016 importedOn "2016-02-19" NP851647.RARishl5Td1Uffxf0-PcHfHmGF20lBwx-dyiqTsQCTa9s130_provenance.