Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_assertion type Assertion NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_head.
- NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_assertion wasGeneratedBy ECO_0000203 NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_provenance.
- NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_assertion wasDerivedFrom befree-2016 NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_provenance.
- NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_assertion SIO_000772 20198651 NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_provenance.
- NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_assertion evidence source_evidence_literature NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_provenance.
- NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_assertion description "[Our data indicate that the FOXL2 codon 134 mutation occurs exclusively in GCT and thecoma, and suggest the possibility that the development of most GCTs and a fraction of thecomas may be dependent on this mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797456.RA5Auh0v5GMi4nduiasYnzw-jANgleZX2Bnd2MuPDsWhg130_provenance.