Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance.
- NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_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." NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance.
- NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_assertion evidence source_evidence_literature NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance.
- NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_assertion SIO_000772 15376319 NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance.
- NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_assertion wasDerivedFrom befree-2016 NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance.
- NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_assertion wasGeneratedBy ECO_0000203 NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP460602.RAzRwxqT9ToCWwwSU1Spvg6V0-8kV7Fd2CNLasGnCVpRQ130_provenance.