Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance.
- NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_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." NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance.
- NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_assertion evidence source_evidence_literature NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance.
- NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_assertion SIO_000772 10814524 NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance.
- NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_assertion wasDerivedFrom befree-20140225 NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance.
- NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_assertion wasGeneratedBy ECO_0000203 NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP181052.RA6PdT8aMnE1RXaSF2jA4U1qt2khXgf-gFmfyqt24gJt8130_provenance.