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- source_evidence_literature type ECO_0000212 NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_provenance.
- NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_assertion description "[HGPS (Hutchinson-Gilford progeria syndrome) is a rare genetic disease affecting children causing them to age and die prematurely.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_provenance.
- NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_assertion evidence source_evidence_literature NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_provenance.
- NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_assertion SIO_000772 20074076 NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_provenance.
- NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_assertion wasDerivedFrom befree-2016 NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_provenance.
- NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_assertion wasGeneratedBy ECO_0000203 NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_provenance.
- befree-2016 importedOn "2016-02-19" NP787060.RAby2kR5eZFjSaf_6-XoPwNJAlW6aRpdsXqRgEOeNg69I130_provenance.