Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance.
- NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_assertion description "[Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance.
- NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_assertion evidence source_evidence_literature NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance.
- NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_assertion SIO_000772 19255821 NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance.
- NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_assertion wasDerivedFrom gad-20150221 NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance.
- NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_assertion wasGeneratedBy ECO_0000203 NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP61388.RAw-bxIe1Jqs8KpQS4P-OhqNbTbCrL5dJA9cJ-0DMXxEc130_provenance.