Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_assertion type Assertion NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_head.
- NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_assertion description "[Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_provenance.
- NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_assertion evidence source_evidence_literature NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_provenance.
- NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_assertion SIO_000772 25105228 NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_provenance.
- NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_assertion wasDerivedFrom befree-20150227 NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_provenance.
- NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_assertion wasGeneratedBy ECO_0000203 NP932877.RAcAVqzSvJm7nnkSPJyh1bEmh0FRljwr4UQD769dmZeF0130_provenance.