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- source_evidence_literature type ECO_0000212 NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_provenance.
- NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_assertion description "[Mutations in RPGR account for over 70% of X-linked retinitis pigmentosa (XlRP), characterized by retinal degeneration and eventual blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_provenance.
- NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_assertion evidence source_evidence_literature NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_provenance.
- NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_assertion SIO_000772 21857984 NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_provenance.
- NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_assertion wasDerivedFrom befree-20150227 NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_provenance.
- NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_assertion wasGeneratedBy ECO_0000203 NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674484.RAhnkoYxwmGA3g8xB7jybAQoxcg7wrlj4SzFO5p7WgJYo130_provenance.