Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_assertion type Assertion NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_head.
- NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_assertion description "[Furthermore, we discuss possible explanations for the phenotypic differences between EEM and congenital hypotrichosis with juvenile macular dystrophy (HJMD), which is also caused by CDH3 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_provenance.
- NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_assertion evidence source_evidence_literature NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_provenance.
- NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_assertion SIO_000772 15805154 NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_provenance.
- NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_assertion wasDerivedFrom befree-20140225 NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_provenance.
- NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_assertion wasGeneratedBy ECO_0000203 NP212013.RAWXQj_T0J_hkaS7iqMquEHFsDFU8jc-8UMDn3pli_fxU130_provenance.