Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance.
- NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_assertion description "[The results suggest that (1) the gene for chondrodysplasia punctata must lie between the X chromosome pseudoautosomal boundary (PABX) and DXS1145; (2) a gene for mental retardation lies between DXS1145 and the sequence tagged site GS1; and (3) the gene for ocular albinism type 1 lies proximal to the STS G13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance.
- NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_assertion evidence source_evidence_literature NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance.
- NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_assertion SIO_000772 7789987 NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance.
- NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_assertion wasDerivedFrom befree-20140225 NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance.
- NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_assertion wasGeneratedBy ECO_0000203 NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP549996.RASH2E_GzabA3jK_mKtxfzPJWCUjCUWV8o7ATQfPpYCUY130_provenance.