Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance.
- NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_assertion description "[Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance.
- NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_assertion evidence source_evidence_literature NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance.
- NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_assertion SIO_000772 20718043 NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance.
- NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_assertion wasDerivedFrom gad-20150221 NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance.
- NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_assertion wasGeneratedBy ECO_0000203 NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance.
- gad-20150221 importedOn "2015-02-21" NP149873.RAfV97zxrRHG10-6z8o2FjEHW46YNMbWlKNpt0jtJH-Ic130_provenance.