Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance.
- NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_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." NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance.
- NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_assertion evidence source_evidence_literature NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance.
- NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_assertion SIO_000772 21109226 NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance.
- NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_assertion wasDerivedFrom befree-2016 NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance.
- NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_assertion wasGeneratedBy ECO_0000203 NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance.
- befree-2016 importedOn "2016-02-19" NP854917.RANoimBVpzz79S6n-A9_tXrHwi-RsgCmpGMXv3rwBVWao130_provenance.