Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_assertion> ?p ?o ?g. }
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- NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_assertion type Assertion NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_head.
- NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_assertion wasGeneratedBy ECO_0000203 NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_provenance.
- NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_assertion wasDerivedFrom befree-20150227 NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_provenance.
- NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_assertion SIO_000772 22279047 NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_provenance.
- NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_assertion evidence source_evidence_literature NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_provenance.
- NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_assertion description "[SMARCAL1 mutations that cause Schimke immunoosseous dysplasia or that inactivate the HARP2 domain abrogate these activities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897258.RAC68AHWQvyUo96BFYq71Xhmlbe7e2-TfZRaxf5nUXdgc130_provenance.