Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_assertion> ?p ?o ?g. }
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- NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_assertion type Assertion NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_head.
- NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_assertion description "[Point mutations in TBX1 can recapitulate many of the structural defects of 22q11 deletion syndromes (22q11DS), usually associated with a chromosomal deletion at 22q1.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_provenance.
- NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_assertion evidence source_evidence_literature NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_provenance.
- NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_assertion SIO_000772 19247433 NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_provenance.
- NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_assertion wasDerivedFrom befree-20140225 NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_provenance.
- NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_assertion wasGeneratedBy ECO_0000203 NP420357.RAcdwgSYx9LTluD-xhUKYmvbYhM_XfpFRn8yy_Xp-iFWc130_provenance.