Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_assertion> ?p ?o ?g. }
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- NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_assertion type Assertion NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_head.
- NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_assertion description "[The H19 gene is abundantly expressed by the human placenta and is implicated in the pathogenesis of congenital growth disorders such as Beckwith-Wiedemann (BWS) and Silver-Russell (SRS) syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_provenance.
- NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_assertion evidence source_evidence_literature NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_provenance.
- NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_assertion SIO_000772 21129773 NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_provenance.
- NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_assertion wasDerivedFrom befree-20140225 NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_provenance.
- NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_assertion wasGeneratedBy ECO_0000203 NP323340.RAZBzjLiOcdeN5IgwcunEjFr0BZP-UUCeMbwTyAGPKRYQ130_provenance.