Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance.
- NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_assertion description "[At least 10 well-defined clinical entities, including Ohtahara, Partington, and Proud syndromes, X-linked infantile spasms, X-linked lissencephaly with ambiguous genitalia, X-linked myoclonic epilepsy and nonsyndromic intellectual disability have been ascertained from among the patients with ARX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance.
- NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_assertion evidence source_evidence_literature NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance.
- NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_assertion SIO_000772 20506206 NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance.
- NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_assertion wasDerivedFrom befree-20140225 NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance.
- NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_assertion wasGeneratedBy ECO_0000203 NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP841682.RAtTxmuXMUWGt_U8nriEna_rLxAw-DixPoKvx4hc_vndw130_provenance.