Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance.
- NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_assertion wasGeneratedBy ECO_0000203 NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance.
- NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_assertion wasDerivedFrom befree-2016 NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance.
- NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_assertion SIO_000772 23178272 NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance.
- NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_assertion evidence source_evidence_literature NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance.
- NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_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." NP1030764.RA6PaptMX210UxHpSFRib7HfTgTOu-nPJOnsEjE2B7o5c130_provenance.