Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance.
- NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_assertion description "[The DNA sequences housing these deletions were found to be putative cis-regulatory elements for Sp1 at CG3 and CG10, and ZNF202 at CG12-16.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance.
- NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_assertion evidence source_evidence_literature NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance.
- NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_assertion SIO_000772 19148275 NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance.
- NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_assertion wasDerivedFrom befree-20140225 NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance.
- NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_assertion wasGeneratedBy ECO_0000203 NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP247008.RAX9ukToL7ecHOqLpNzF9XSPZAUV7zhcf-Ch3bBH9qmlY130_provenance.