Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_assertion> ?p ?o ?g. }
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- NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_assertion type Assertion NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_head.
- NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_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." NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_provenance.
- NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_assertion evidence source_evidence_literature NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_provenance.
- NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_assertion SIO_000772 15705923 NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_provenance.
- NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_assertion wasDerivedFrom befree-20150227 NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_provenance.
- NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_assertion wasGeneratedBy ECO_0000203 NP419241.RAmEIWtn7qjMTAx-NeW0bD5RwIhE9WJF_TqIuZontYCvg130_provenance.