Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance.
- NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_assertion description "[Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance.
- NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_assertion evidence source_evidence_literature NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance.
- NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_assertion SIO_000772 15376319 NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance.
- NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_assertion wasDerivedFrom befree-20140225 NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance.
- NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_assertion wasGeneratedBy ECO_0000203 NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP267891.RAsE_fppPGT5Ln7wFOXl-1PmGt4Lsr6GBwqMphKTmEkOk130_provenance.