Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance.
- NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_assertion description "[Mutations in the human RDS gene are responsible for several forms of inherited blindness including autosomal-dominant retinitis pigmentosa and macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance.
- NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_assertion evidence source_evidence_literature NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance.
- NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_assertion SIO_000772 10704489 NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance.
- NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_assertion wasDerivedFrom befree-2016 NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance.
- NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_assertion wasGeneratedBy ECO_0000203 NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance.
- befree-2016 importedOn "2016-02-19" NP277189.RAaSNA0MDcCGqe1mXldKzjDSIL7qqS_p2lBxVOg0TXBng130_provenance.