Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion description "[We describe prenatal genetic testing of FGFR2 in a fetus of a mother whose previous child had Crouzon Syndrome due to an apparently de novo mutation, S351C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion evidence source_evidence_literature NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion SIO_000772 15916101 NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion wasDerivedFrom befree-20140225 NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_assertion wasGeneratedBy ECO_0000203 NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP382329.RAg7JjOXt_Oocjab6Xbt2kW55Gf_AWsLI_CV5C1ZVWXFU130_provenance.