Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance.
- NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_assertion description "[Autosomal recessive (AR) EVER1 and EVER2 deficiencies account for two thirds of known cases of EV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance.
- NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_assertion evidence source_evidence_literature NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance.
- NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_assertion SIO_000772 22952854 NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance.
- NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_assertion wasDerivedFrom befree-2016 NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance.
- NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_assertion wasGeneratedBy ECO_0000203 NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1010725.RAngTUGVhrRfiPdbDJg106ucD9vvDbOQURHu3Ce9OZyAI130_provenance.