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- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion type Assertion NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_head.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion description "[Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion evidence source_evidence_literature NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion SIO_000772 15705923 NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion wasDerivedFrom befree-20140225 NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.
- NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_assertion wasGeneratedBy ECO_0000203 NP713898.RAoT4PnEPAUSz6J23YLMzb00QOJXKRcMjRM4QHgr1rEpw130_provenance.