Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_assertion> ?p ?o ?g. }
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- NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_assertion type Assertion NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_head.
- NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_assertion wasGeneratedBy ECO_0000203 NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_provenance.
- NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_assertion wasDerivedFrom befree-20140225 NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_provenance.
- NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_assertion SIO_000772 23787483 NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_provenance.
- NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_assertion evidence source_evidence_literature NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_provenance.
- NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_assertion description "[A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565886.RAQ77pYQWxLGeUVzgzA4s_3O28WvH8Bs76YbVZ7bAZpiU130_provenance.