Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_assertion type Assertion NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_head.
- NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_assertion description "[Interestingly the ALP gene occurs at 4q35 near the heterochromatic region mutated in facioscapulohumeral muscular dystrophy, indicating a possible role for ALP in this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_provenance.
- NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_assertion evidence source_evidence_literature NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_provenance.
- NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_assertion SIO_000772 11238905 NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_provenance.
- NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_assertion wasDerivedFrom befree-20140225 NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_provenance.
- NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_assertion wasGeneratedBy ECO_0000203 NP221912.RAUAaXbbS4HfdUba28RsbY1FX8JfgEvkODEFPEJd1v_Zo130_provenance.