Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance.
- NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_assertion description "[In this study, we performed comprehensive genetic analysis of the RP-C4-CYP21-TNX (RCCX) region in 127 unrelated 21-OHD patients (100 classic, 27 nonclassic).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance.
- NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_assertion evidence source_evidence_literature NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance.
- NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_assertion SIO_000772 22886582 NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance.
- NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_assertion wasDerivedFrom befree-20140225 NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance.
- NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_assertion wasGeneratedBy ECO_0000203 NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP610728.RAfJhXffvFKA9p1EQJhcUxO_9SWhdnF4EHWRymJhs5OAo130_provenance.