Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_assertion> ?p ?o ?g. }
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- NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_assertion type Assertion NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_head.
- NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_assertion description "[Heterozygote deletions or mutations of pseudoautosomal 1 region (PAR1) encompassing the short stature homeobox-containing (SHOX) gene cause Leri-Weill Dyschondrosteosis (LWD), which is a dominantly inherited osteochondroplasia characterized by short stature with mesomelic shortening of the upper and lower limbs and Madelung deformity of the wrists.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_provenance.
- NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_assertion evidence source_evidence_literature NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_provenance.
- NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_assertion SIO_000772 19400538 NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_provenance.
- NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_assertion wasDerivedFrom befree-20150227 NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_provenance.
- NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_assertion wasGeneratedBy ECO_0000203 NP943742.RA81I2UGuujWxN3uwCbydk6fNiJ4FocDnXxgc3wNtFe30130_provenance.