Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance.
- NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_assertion description "[However, unlike the Apert syndrome Pro253Arg FGFR2c mutant, neither the Pfeiffer syndrome Pro250Arg FGFR1c mutant nor the Muenke syndrome Pro250Arg FGFR3c mutant bound appreciably to FGF7 or FGF10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance.
- NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_assertion evidence source_evidence_literature NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance.
- NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_assertion SIO_000772 14613973 NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance.
- NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_assertion wasDerivedFrom befree-2016 NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance.
- NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_assertion wasGeneratedBy ECO_0000203 NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP420425.RAu_2YXj6pPe7DyLUHwpybkg5RYsvoi0E8-x-iynX62eQ130_provenance.