Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance.
- NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_assertion description "[To address these issues, we genotyped SNPs in ANK3, CACNA1C, CMTM8, DGKH, EGFR, and NPAS3, which were significantly associated with BPD in previous GWAS, in a sample of 380 BPD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance.
- NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_assertion evidence source_evidence_literature NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance.
- NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_assertion SIO_000772 21654738 NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance.
- NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_assertion wasDerivedFrom befree-2016 NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance.
- NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_assertion wasGeneratedBy ECO_0000203 NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP900426.RAxiAjIh1hqLKIYDrd6AZWY1Urx4fJKrf4oqFY9i4ZjDQ130_provenance.