Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_assertion> ?p ?o ?g. }
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- NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_assertion type Assertion NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_head.
- NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_assertion wasGeneratedBy ECO_0000203 NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_provenance.
- NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_assertion wasDerivedFrom befree-20150227 NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_provenance.
- NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_assertion SIO_000772 20584796 NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_provenance.
- NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_assertion evidence source_evidence_literature NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_provenance.
- NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_assertion description "[Defects of the NKX2-1 gene, encoding thyroid transcription factor-1, cause brain-thyroid-lung syndrome (MIM 610978), characterised by benign hereditary chorea, congenital hypothyroidism and respiratory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP739275.RAFAX4pT4wFgPsvuILO_EjxSR7f1W9XP6to3fFAzZCQ_I130_provenance.