Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance.
- NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_assertion description "[Significantly, these abnormalities are similar to the skeletal anomalies found in trisomy-16 mice and in humans with Down's syndrome, wherein the dosage of Ets2 is known to be increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance.
- NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_assertion evidence source_evidence_literature NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance.
- NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_assertion SIO_000772 11175361 NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance.
- NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_assertion wasDerivedFrom befree-20150227 NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance.
- NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_assertion wasGeneratedBy ECO_0000203 NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP386519.RAthiPX51UDqraTiquArMTm8iYSIPotsY6TZ-R6X-dwlw130_provenance.