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- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion type Assertion NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_head.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion description "[The TBX1 gene is considered to be the major candidate gene for the main features in 22q11.2 deletion syndrome, including congenital heart malformations, (para)thyroid hypoplasia, and craniofacial abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion evidence source_evidence_literature NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion SIO_000772 22893440 NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion wasDerivedFrom befree-20140225 NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.
- NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_assertion wasGeneratedBy ECO_0000203 NP346418.RAJiozHRUh9_cqY1KmsXF4YlfChfLeq4ywI69N2IoKsO4130_provenance.