Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_assertion> ?p ?o ?g. }
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- NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_assertion type Assertion NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_head.
- NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_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." NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_provenance.
- NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_assertion evidence source_evidence_literature NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_provenance.
- NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_assertion SIO_000772 15705923 NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_provenance.
- NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_assertion wasDerivedFrom befree-2016 NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_provenance.
- NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_assertion wasGeneratedBy ECO_0000203 NP480539.RA4MKbmdgVMLNvgbgRD0hJCnmzRuLwgzPdKwZnxk2vIEM130_provenance.