Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance.
- NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_assertion description "[CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance.
- NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_assertion evidence source_evidence_literature NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance.
- NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_assertion SIO_000772 19461874 NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance.
- NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_assertion wasDerivedFrom befree-20140225 NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance.
- NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_assertion wasGeneratedBy ECO_0000203 NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP721222.RASS2QyBx2hh9TPdoDclpP7CbW4SRrUU_PBlYgw_EMIMM130_provenance.