Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance.
- NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_assertion wasGeneratedBy ECO_0000203 NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance.
- NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_assertion wasDerivedFrom befree-20150227 NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance.
- NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_assertion SIO_000772 10698592 NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance.
- NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_assertion evidence source_evidence_literature NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance.
- NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_assertion description "[The identification of the gene(s) causing FGD without mutations in the MC2-R and causing the triple A syndrome may reveal novel aspects in cell signalling and neuroendocrinology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548248.RAVfY9E5hMq7nygZ_94q-xCq5qYrHcDR9GiJC8Z-WIWOE130_provenance.