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- NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_assertion type Assertion NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_head.
- NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_assertion wasGeneratedBy ECO_0000203 NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_provenance.
- NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_assertion wasDerivedFrom befree-20140225 NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_provenance.
- NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_assertion SIO_000772 16912130 NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_provenance.
- NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_assertion evidence source_evidence_literature NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_provenance.
- NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_assertion description "[Identification of three novel mutations in the GATA3 gene responsible for familial hypoparathyroidism and deafness in the Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614713.RAhtC6C1Z-LXL9-MTJ520r1u18SnYl6bVNLjWaWjZYi5o130_provenance.