Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_assertion type Assertion NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_head.
- NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_assertion description "[We used exome sequencing, Sanger sequencing, and copy number analysis to screen 65 unrelated individuals with schwannomatosis who were negative for a germline NF2 or SMARCB1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_provenance.
- NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_assertion evidence source_evidence_literature NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_provenance.
- NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_assertion SIO_000772 25480913 NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_provenance.
- NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_assertion wasDerivedFrom befree-2016 NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_provenance.
- NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_assertion wasGeneratedBy ECO_0000203 NP1245379.RARJfnUiKgzbDjEjeuuCSLbka_dIzg24qcp8IXlgS2jv0130_provenance.