Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance.
- NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_assertion description "[The crystal structure, of Pro252Arg FGFR1c in complex with FGF2, demonstrates that the enhanced ligand binding is due to an additional set of receptor-ligand hydrogen bonds, similar to those gain-of-function interactions that occur in the Apert syndrome Pro253Arg FGFR2c-FGF2 crystal structure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance.
- NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_assertion evidence source_evidence_literature NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance.
- NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_assertion SIO_000772 14613973 NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance.
- NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_assertion wasDerivedFrom befree-20150227 NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance.
- NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_assertion wasGeneratedBy ECO_0000203 NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP399862.RAC4qxOCHeZ5jmmQUifTGU_vXkVIRGLfAv5o5fDwoMZPM130_provenance.