Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance.
- NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_assertion description "[Aristaless-related homeobox gene disruption leads to abnormal distribution of GABAergic interneurons in human neocortex: evidence based on a case of X-linked lissencephaly with abnormal genitalia (XLAG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance.
- NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_assertion evidence source_evidence_literature NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance.
- NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_assertion SIO_000772 18458920 NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance.
- NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_assertion wasDerivedFrom befree-20140225 NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance.
- NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_assertion wasGeneratedBy ECO_0000203 NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP220781.RADfYrxDy5F2ff25Hycxr1K18zLEvRbk-OL0jm-PTe7UA130_provenance.