Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance.
- NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_assertion wasGeneratedBy ECO_0000203 NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance.
- NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_assertion wasDerivedFrom befree-20150227 NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance.
- NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_assertion SIO_000772 23178272 NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance.
- NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_assertion evidence source_evidence_literature NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance.
- NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_assertion description "[STUDY DESIGN, MATERIAL AND METHODS: We conducted a case-control study using population-based data from the Paris registry of congenital malformations for the period 1987-2009 and a cohort study of CHD (EPICARD) on 1583 cases of CHDs and 4104 malformed controls with no known associations with ARTs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918189.RAYokCQsPZpMQYyM5a1YwOJACzp-kLYD7Gr2bMeNt1mh8130_provenance.