Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance.
- NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_assertion description "[Paediatric GH is currently licensed in six different conditions: growth hormone deficiency (GHD), Turner syndrome (TS), small for gestational age (SGA), Prader-Willi-syndrome (PWS), chronic renal insufficiency (CRI), and short stature due to SHOX deficiency; all of these have been ratified by the most recent (2010) NICE review.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance.
- NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_assertion evidence source_evidence_literature NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance.
- NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_assertion SIO_000772 21540481 NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance.
- NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_assertion wasDerivedFrom befree-2016 NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance.
- NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_assertion wasGeneratedBy ECO_0000203 NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP891540.RARjvrOeV0pExkQJu3vNpGIoU7M-KcNQ8BE4u10a8GTR0130_provenance.