Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_assertion> ?p ?o ?g. }
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- NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_assertion type Assertion NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_head.
- NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_assertion description "[The hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an autosomal dominant disorder caused by mutations of a member of the GATA-binding family of transcription factors, GATA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_provenance.
- NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_assertion evidence source_evidence_literature NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_provenance.
- NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_assertion SIO_000772 15705923 NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_provenance.
- NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_assertion wasDerivedFrom befree-20150227 NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_provenance.
- NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_assertion wasGeneratedBy ECO_0000203 NP917594.RAi8bCWLVc1ewNYsjpuaUz37z2WcfajtTe_pEWDpq1aRw130_provenance.