Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance.
- NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_assertion description "[PITX2 mutations are known to be responsible for Axenfield Rieger syndrome, a genetic disorder in which pituitary abnormalities have been detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance.
- NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_assertion evidence source_evidence_literature NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance.
- NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_assertion SIO_000772 21810944 NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance.
- NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_assertion wasDerivedFrom befree-2016 NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance.
- NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_assertion wasGeneratedBy ECO_0000203 NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance.
- befree-2016 importedOn "2016-02-19" NP914255.RA9lkt7OUYsu46OQMvMQNysGp5z8FzRdqSpPI1KVsxzbY130_provenance.