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- source_evidence_literature type ECO_0000212 NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_provenance.
- NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_assertion description "[The authors report a novel 24-bp in-frame deletion within exon 2 of the ARX gene in a male child with X-linked mental retardation and review the spectrum of ARX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_provenance.
- NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_assertion evidence source_evidence_literature NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_provenance.
- NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_assertion SIO_000772 17641262 NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_provenance.
- NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_assertion wasDerivedFrom befree-20150227 NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_provenance.
- NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_assertion wasGeneratedBy ECO_0000203 NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835548.RAB7lQ6vlGzixgt5MfW1335LfKFhOzJOY-JDg23LDACGw130_provenance.