Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance.
- NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_assertion description "[We have isolated two novel genes, designated DSCR5 and DSCR6, from the Down syndrome critical region (DSCR) on chromosome 21q22.2 which has been defined as minimal overlapping region of partial trisomy 21 patients and located between t(4;21) break point and ERG (approximately 1.6 Mb).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance.
- NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_assertion evidence source_evidence_literature NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance.
- NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_assertion SIO_000772 10814524 NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance.
- NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_assertion wasDerivedFrom befree-20140225 NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance.
- NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_assertion wasGeneratedBy ECO_0000203 NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP731908.RABFKT108AvrCCfMQRMbSmeoUrd58BdK4SUp4LhBU_yUM130_provenance.