Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance.
- NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_assertion description "[We tested genomic deoxyribonucleic acid from 608 prospectively recruited patients with conotruncal anomalies (n = 370), left-sided lesions (n = 160), secundum atrial septal defect (ASD) (n = 71), and Ebstein's malformation (n = 7) for NKX2.5 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance.
- NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_assertion evidence source_evidence_literature NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance.
- NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_assertion SIO_000772 14607454 NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance.
- NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_assertion wasDerivedFrom befree-20150227 NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance.
- NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_assertion wasGeneratedBy ECO_0000203 NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333966.RAgMTJ08_ycevLvS21Jaoh1I9byNI5Y-qcJVs8dK_HYAI130_provenance.