Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance.
- NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_assertion description "[Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance.
- NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_assertion evidence source_evidence_literature NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance.
- NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_assertion SIO_000772 18779497 NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance.
- NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_assertion wasDerivedFrom befree-20150227 NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance.
- NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_assertion wasGeneratedBy ECO_0000203 NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974170.RAVuAWnLGKBJkTs8mW1gsMW4TshYXmjHpdIs7Gzn8jUqA130_provenance.