Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance.
- befree-20150227 importedOn "2015-02-27" NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance.
- NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_assertion wasGeneratedBy ECO_0000203 NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance.
- NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_assertion wasDerivedFrom befree-20150227 NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance.
- NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_assertion SIO_000772 22038540 NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance.
- NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_assertion evidence source_evidence_literature NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance.
- NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_assertion description "[The chromatin remodelling gene SMARCB1 (also known as INI1, hSNF5, and BAF47) has been identified as a schwannomatosis predisposing gene, being involved in a subset of sporadic and familial cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP703311.RAPSUUXcBfClBMAL0Rk_NQ1STfsM8WsqUuYtfd8ysLa38130_provenance.