Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance.
- NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_assertion description "[Mutations in the human aristaless-related homeobox (ARX) gene are amongst the major causes of developmental and neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance.
- NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_assertion evidence source_evidence_literature NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance.
- NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_assertion SIO_000772 22642246 NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance.
- NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_assertion wasDerivedFrom befree-20140225 NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance.
- NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_assertion wasGeneratedBy ECO_0000203 NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP197028.RAy_8tdD3ItvWad-wXU36NRnImILbbB3b2aQywH0DkN_4130_provenance.