Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance.
- befree-2016 importedOn "2016-02-19" NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance.
- NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_assertion wasGeneratedBy ECO_0000203 NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance.
- NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_assertion wasDerivedFrom befree-2016 NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance.
- NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_assertion SIO_000772 19243295 NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance.
- NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_assertion evidence source_evidence_literature NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance.
- NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_assertion description "[The majority of the mutations identified are identical to germline mutations in FGFR2 and FGFR3 that cause craniosynostosis and hypochondroplasia syndromes and result in both ligand-independent and ligand-dependent receptor activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722541.RAR8g7R74b8vd6ckQIeDGPFHfJwqsGrPvefSXkSYVyxdE130_provenance.