Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance.
- NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_assertion description "[The maternal MTHFR 677C > T variants are a risk factor for CHD in offspring, confined to conotruncal heart defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance.
- NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_assertion evidence source_evidence_curated NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance.
- NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_assertion SIO_000772 16524890 NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance.
- NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_assertion wasDerivedFrom ctd_human-20130708 NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance.
- NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_assertion wasGeneratedBy ECO_0000218 NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP23402.RAAwKK6xDMm3uAT6sZtOuqgK6eR-e2XMW3eIkiELkxhew130_provenance.