Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_assertion> ?p ?o ?g. }
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- NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_assertion type Assertion NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_head.
- NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_assertion wasGeneratedBy ECO_0000203 NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_provenance.
- NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_assertion wasDerivedFrom befree-2016 NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_provenance.
- NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_assertion SIO_000772 20718765 NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_provenance.
- NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_assertion evidence source_evidence_literature NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_provenance.
- NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_assertion description "[Characterization of a novel loss-of-function mutation of PAX8 associated with congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833508.RAPI0FsUf8vqYgLQ4BzCv07TEZToF0Fjgg-vMQhsuhLsc130_provenance.