Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance.
- NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_assertion description "[These data suggest that potentially pathogenic ROM1 mutations occur in 1% or less of patients with adRP or simplex RP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance.
- NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_assertion evidence source_evidence_literature NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance.
- NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_assertion SIO_000772 8595413 NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance.
- NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_assertion wasDerivedFrom befree-20140225 NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance.
- NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_assertion wasGeneratedBy ECO_0000203 NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563109.RAjpiIv6n3sEAqyQ7erpcxXO352P34l8zit3joekJ5-KU130_provenance.