Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance.
- NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_assertion wasGeneratedBy ECO_0000203 NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance.
- NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_assertion wasDerivedFrom befree-2016 NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance.
- NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_assertion SIO_000772 9661624 NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance.
- NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_assertion evidence source_evidence_literature NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance.
- NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_assertion description "[We also identified the previously described Ala568Val mutation in the third intracellular loop of the LHR in the other affected African-Brazilian boy and his normal prepubertal sister, suggesting the inherited form of precocious puberty in this boy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1399140.RAaW16-RMWxd7vcWyF1vH5QMEFLCgXGqWcUdG_9ITQ17U130_provenance.