Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance.
- NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_assertion description "[The linkage region has been refined to a 24 cM region between D14S283 and D14S49 and mutations have been excluded in the PABP2 gene for oculopharyngeal muscular dystrophy which lies within this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance.
- NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_assertion evidence source_evidence_literature NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance.
- NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_assertion SIO_000772 12062252 NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance.
- NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_assertion wasDerivedFrom befree-20140225 NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance.
- NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_assertion wasGeneratedBy ECO_0000203 NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP616174.RAZ40o4hLECU15AgfUJjNVe4YR7GIWyhJhz3S9JLEbryQ130_provenance.