Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance.
- 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.
- gad-20130706 importedOn "2013-07-06" NP62860.RAkJ6ejPNAMnSQCl9Yiw3bwgcxTDOh_Rk3niJgZtOrYHY130_provenance.