Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_assertion> ?p ?o ?g. }
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- NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_assertion type Assertion NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_head.
- NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_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." NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_provenance.
- NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_assertion evidence source_evidence_literature NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_provenance.
- NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_assertion SIO_000772 19400538 NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_provenance.
- NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_assertion wasDerivedFrom befree-20150227 NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_provenance.
- NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_assertion wasGeneratedBy ECO_0000203 NP808806.RAWa6CbxhlJ9GNVHrQaDTPnfxwhhoxjeNMoqwcz1I5eoQ130_provenance.