Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_assertion> ?p ?o ?g. }
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- NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_assertion type Assertion NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_head.
- NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_assertion wasGeneratedBy ECO_0000203 NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_provenance.
- NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_assertion wasDerivedFrom befree-2016 NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_provenance.
- NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_assertion SIO_000772 9590296 NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_provenance.
- NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_assertion evidence source_evidence_literature NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_provenance.
- NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_assertion description "[PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395363.RA20gSfrlhRu2SQLSYVQrrzDL0A82dXyUN0USXXjjgVUI130_provenance.