Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_assertion> ?p ?o ?g. }
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- NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_assertion type Assertion NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_head.
- NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_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." NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_provenance.
- NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_assertion evidence source_evidence_literature NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_provenance.
- NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_assertion SIO_000772 21270324 NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_provenance.
- NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_assertion wasDerivedFrom befree-20140225 NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_provenance.
- NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_assertion wasGeneratedBy ECO_0000203 NP886375.RAimg4xz6pGvL8GubUmD69UWSYJ1cd5zOj6LQS5SjzVTU130_provenance.