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- source_evidence_literature type ECO_0000212 NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.
- NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.
- NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_assertion evidence source_evidence_literature NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.
- NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_assertion SIO_000772 16724181 NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.
- NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_assertion wasDerivedFrom befree-2016 NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.
- NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_assertion wasGeneratedBy ECO_0000203 NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.
- befree-2016 importedOn "2016-02-19" NP551514.RASH_uhRO1-UftTcQjnAQZ6YQniNiRWL3oWIAOadzkwfA130_provenance.