Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance.
- NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_assertion description "[Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance.
- NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_assertion evidence source_evidence_literature NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance.
- NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_assertion SIO_000772 21109226 NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance.
- NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_assertion wasDerivedFrom befree-20150227 NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance.
- NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_assertion wasGeneratedBy ECO_0000203 NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP450326.RA-gtMpbdb6bBM8GbGL2tXfPVA59ZifZtlm9i-OTjsFnM130_provenance.