Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance.
- NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_assertion description "[In conclusion, MTRR 66 GG and TC 776 GG genotypes in mothers and children may contribute to the risk of CHDs, particularly when the maternal vitamin B12 status is low.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance.
- NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_assertion evidence source_evidence_literature NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance.
- NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_assertion SIO_000772 18226574 NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance.
- NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_assertion wasDerivedFrom gad-20150221 NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance.
- NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_assertion wasGeneratedBy ECO_0000203 NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP149144.RAr2lKXGXhlfbYvTtX4NOhkNgVUAhhiGTZeVBf9ephfMw130_provenance.