Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance.
- NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_assertion description "[Mutations in the retinitis pigmentosa 1 (RP1) gene are a common cause of autosomal dominant retinitis pigmentosa (adRP), and have also been found to cause autosomal recessive RP (arRP) in a few families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance.
- NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_assertion evidence source_evidence_literature NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance.
- NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_assertion SIO_000772 22927954 NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance.
- NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_assertion wasDerivedFrom befree-20140225 NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance.
- NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_assertion wasGeneratedBy ECO_0000203 NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476560.RAL0foX2AwRZjzGInKuZWvNbIHLPo94kbXNVZWwzgp1-M130_provenance.