Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance.
- NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_assertion description "[FOXC2 represents the second known gene to result in hereditary lymphedema, and LD is only the second hereditary disorder known to be caused by a mutation in a forkhead-family gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance.
- NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_assertion evidence source_evidence_literature NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance.
- NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_assertion SIO_000772 11078474 NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance.
- NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_assertion wasDerivedFrom befree-20140225 NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance.
- NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_assertion wasGeneratedBy ECO_0000203 NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP756808.RAVWXnUS0oU3rNIt5IPzYXwuRXtCzYkNdoy3Ca6la2GYw130_provenance.