Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_assertion> ?p ?o ?g. }
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- NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_assertion type Assertion NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_head.
- NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_assertion description "[To determine whether mutations in these genes cause spontaneous cervical artery dissection (sCAD), all coding exons of TGFBR1 and TGFBR2 were sequenced in 56 consecutive patients with sCAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_provenance.
- NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_assertion evidence source_evidence_literature NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_provenance.
- NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_assertion SIO_000772 21270064 NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_provenance.
- NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_assertion wasDerivedFrom befree-20140225 NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_provenance.
- NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_assertion wasGeneratedBy ECO_0000203 NP922107.RA9mMXIhFyxw_etOkoZ5dbHAvx2NsqrAm-ZxqleGohotA130_provenance.