Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance.
- NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_assertion description "[Genetic disorders in humans have been identified that render DBH, and the NET dysfunctional and result in cardiovascular and neurological abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance.
- NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_assertion evidence source_evidence_literature NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance.
- NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_assertion SIO_000772 14730204 NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance.
- NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_assertion wasDerivedFrom befree-20140225 NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance.
- NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_assertion wasGeneratedBy ECO_0000203 NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP756798.RAN0_B1IVlXT-mDTgJ63IIVMyYms5XGKLs04wLYxtGwWs130_provenance.