Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance.
- NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_assertion description "[These results suggest that small sequence changes in ANKH are one cause of CC and joint disease in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance.
- NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_assertion evidence source_evidence_literature NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance.
- NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_assertion SIO_000772 12297987 NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance.
- NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_assertion wasDerivedFrom befree-20140225 NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance.
- NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_assertion wasGeneratedBy ECO_0000203 NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance.
- befree-20140225 importedOn "2014-02-25" NP626334.RAeoCvNp5dwbsx1VpDAeY8VGvRZVte0h7LE7OXYk1WE20130_provenance.