Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_assertion type Assertion NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_head.
- NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_assertion description "[Mutations in the zinc finger transcription factor ZIC3 cause X-linked heterotaxy and have also been identified in patients with isolated congenital heart disease (CHD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_provenance.
- NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_assertion evidence source_evidence_literature NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_provenance.
- NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_assertion SIO_000772 14681828 NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_provenance.
- NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_assertion wasDerivedFrom befree-20140225 NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_provenance.
- NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_assertion wasGeneratedBy ECO_0000203 NP485015.RAW1avzsY7ISK_0dIS4FM9zxVqTYnkET2a7LUwGHJY9_o130_provenance.