Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance.
- NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_assertion description "[To evaluate the distribution of polymorphisms in the endothelin 1 (EDN1), endothelin receptor A (EDNRA) and endothelin receptor B (EDNRB) genes in systemic sclerosis (SSc; scleroderma) and SSc subsets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance.
- NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_assertion evidence source_evidence_literature NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance.
- NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_assertion SIO_000772 16947775 NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance.
- NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_assertion wasDerivedFrom befree-20150227 NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance.
- NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_assertion wasGeneratedBy ECO_0000203 NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP364604.RAlRFJH1CmTPpJN8kMwU94FYPPFKjqtlee9chas8t6f-M130_provenance.