Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance.
- NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_assertion description "[Beside FMR1, in families with X-linked mental retardation (XLMR), the ARX dysfunction was demonstrated to be among the most frequent causes of this heterogeneous group of disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance.
- NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_assertion evidence source_evidence_literature NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance.
- NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_assertion SIO_000772 16523516 NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance.
- NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_assertion wasDerivedFrom befree-2016 NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance.
- NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_assertion wasGeneratedBy ECO_0000203 NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance.
- befree-2016 importedOn "2016-02-19" NP539176.RAewRBlAWSdmFqXGnRRpkZ4o5Uqp4TRta5biGbECl8jNY130_provenance.