Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_assertion type Assertion NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_head.
- NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_assertion description "[An array of vastly different diagnoses is caused by similar mutations in FGFR3, including syndromes affecting skeletal development (hypochondroplasia [HCH], ACH, thanatophoric dysplasia [TD]), skin (epidermal nevi, seborrhaeic keratosis, acanthosis nigricans), and cancer (multiple myeloma [MM], prostate and bladder carcinoma, seminoma).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_provenance.
- NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_assertion evidence source_evidence_literature NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_provenance.
- NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_assertion SIO_000772 22045636 NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_provenance.
- NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_assertion wasDerivedFrom befree-20140225 NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_provenance.
- NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_assertion wasGeneratedBy ECO_0000203 NP742161.RAlUq-QLkhVrrabvbJIyKvrTEje5dqjuh_gl8uLWZnNvI130_provenance.