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- source_evidence_literature type ECO_0000212 NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_provenance.
- NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_assertion wasGeneratedBy ECO_0000203 NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_provenance.
- NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_assertion wasDerivedFrom befree-20150227 NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_provenance.
- NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_assertion SIO_000772 15288992 NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_provenance.
- NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_assertion evidence source_evidence_literature NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_provenance.
- NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_assertion description "[This study was conducted to evaluate fundus autofluorescence in patients with early-onset severe retinal dystrophy (EOSRD, or early-onset rod-cone dystrophy) associated with mutations on both alleles of RPE65.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674761.RA6x20yg_TcXyVxitdTwd_TgvnzufHmYvGsTyYdhnLp_0130_provenance.