Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion type Assertion NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_head.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion wasGeneratedBy ECO_0000203 NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion wasDerivedFrom befree-20140225 NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion SIO_000772 23840040 NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion evidence source_evidence_literature NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.
- NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_assertion description "[Mutations in solute carrier family 26 (sulfate transporter), member 2 (SLC26A2) gene result in a spectrum of autosomal recessive chondrodysplasias that range from the mildest recessive form of multiple epiphysial dysplasia (rMED) through the most common diastrophic dysplasia (DTD) to lethal atelosteogenesis type II and achondrogenesis IB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512969.RAbYnbFewOakl1lQlONKJ9oI-Z64MlonoGXKqskxsOLns130_provenance.