Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_assertion type Assertion NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_head.
- NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_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." NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_provenance.
- NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_assertion evidence source_evidence_literature NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_provenance.
- NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_assertion SIO_000772 21540481 NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_provenance.
- NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_assertion wasDerivedFrom befree-2016 NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_provenance.
- NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_assertion wasGeneratedBy ECO_0000203 NP891543.RAt7BJWnS_iiF64a6fMand5b5PbLEEE6Awmljf65_npcY130_provenance.