Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance.
- NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_assertion description "[In a small group of patients the identification of a constitutional deletion on the long arm of chromosome 13 indicated the location of the critical gene in region 13q14 Close linkage between the hereditary, non-deletion form of RB and the esterase-D gene, which is also located in 13q14, demonstrated that all hereditary forms of RB are due to defects in a gene at this locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance.
- NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_assertion evidence source_evidence_literature NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance.
- NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_assertion SIO_000772 2571113 NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance.
- NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_assertion wasDerivedFrom befree-20150227 NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance.
- NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_assertion wasGeneratedBy ECO_0000203 NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP383509.RA7dO1mHYZTsuyV4r3TQj_LSfegVuUtRPir2nADr_8K2E130_provenance.