Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_assertion> ?p ?o ?g. }
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- NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_assertion type Assertion NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_head.
- NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_assertion wasGeneratedBy ECO_0000203 NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_provenance.
- NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_assertion wasDerivedFrom befree-20150227 NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_provenance.
- NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_assertion SIO_000772 25146893 NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_provenance.
- NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_assertion evidence source_evidence_literature NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_provenance.
- NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_assertion description "[Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784311.RAtriWBI1irXYP9YOkuCgJnaNBuZu0u7Y2NYVt_ju3Gco130_provenance.