Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_assertion> ?p ?o ?g. }
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- NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_assertion type Assertion NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_head.
- NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_assertion description "[In syndromic craniosynostosis, there is a highly nonrandom pattern of causative autosomal dominant mutations involving TWIST1 and fibroblast growth factor receptors (FGFRs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance.
- NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_assertion evidence source_evidence_literature NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance.
- NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_assertion SIO_000772 17343269 NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance.
- NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_assertion wasDerivedFrom gad-20130706 NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance.
- NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_assertion wasGeneratedBy ECO_0000203 NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance.