Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance.
- NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_assertion description "[Human norepinephrine (NE) deficiency (or dopamine ?-hydroxylase (DBH) deficiency) is a rare congenital disorder of primary autonomic failure, in which neurotransmitters NE and epinephrine are undetectable.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance.
- NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_assertion evidence source_evidence_literature NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance.
- NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_assertion SIO_000772 21209083 NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance.
- NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_assertion wasDerivedFrom befree-20150227 NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance.
- NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_assertion wasGeneratedBy ECO_0000203 NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP347721.RAd-D5dsRLJ_mARDdKQYIS-XgW4dRqC3OEscPglCwXFsM130_provenance.