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- NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_assertion type Assertion NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_head.
- NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_assertion wasGeneratedBy ECO_0000203 NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_provenance.
- NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_assertion wasDerivedFrom gad-20130706 NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_provenance.
- NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_assertion SIO_000772 12798584 NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_provenance.
- NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_assertion evidence source_evidence_literature NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_provenance.
- NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_assertion description "[Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53887.RADGAx7AzK9JkEID-xRgIYiQLAaI7zuA22VZebUgvhpMU130_provenance.