Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance.
- NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_assertion description "[, we can say that FV 1691 A and PT 20210 A mutations are important and must be included to the routine analysis of pediatric stroke patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance.
- NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_assertion evidence source_evidence_literature NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance.
- NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_assertion SIO_000772 11323021 NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance.
- NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_assertion wasDerivedFrom gad-20150221 NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance.
- NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_assertion wasGeneratedBy ECO_0000203 NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP69914.RAcncaVAnRbWqbOcJ14CITFnot2inkcFw7Egq7OtcWlZk130_provenance.