Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_assertion> ?p ?o ?g. }
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- NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_assertion type Assertion NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_head.
- NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_assertion description "[Klinefelter syndrome (KS) is a chromosomal alteration characterized by supernumerary X-chromosome(s), primary hypogonadism, decreased pubertal peak bone mineral density (BMD), and accelerated bone loss during adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_provenance.
- NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_assertion evidence source_evidence_literature NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_provenance.
- NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_assertion SIO_000772 21270324 NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_provenance.
- NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_assertion wasDerivedFrom befree-20140225 NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_provenance.
- NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_assertion wasGeneratedBy ECO_0000203 NP918925.RAwY_U_cb-4F3td88zZ21ZxXNeZBee58YBzPibKJPUgps130_provenance.