Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_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." NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion evidence source_evidence_literature NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion SIO_000772 15921228 NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion wasDerivedFrom befree-20140225 NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion wasGeneratedBy ECO_0000203 NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.