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- source_evidence_literature type ECO_0000212 NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_provenance.
- NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_assertion description "[We found a non-significant increased risk of being a homozygous MTHFR C677T carrier in the placental abruption group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_provenance.
- NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_assertion evidence source_evidence_literature NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_provenance.
- NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_assertion SIO_000772 17627684 NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_provenance.
- NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_assertion wasDerivedFrom lhgdn-20090331 NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_provenance.
- NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_assertion wasGeneratedBy ECO_0000203 NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP211517.RAsQXLhcbAQqvxdfkvePcC4kWyp2NNEUys-kBQbnCusCo130_provenance.