Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_assertion> ?p ?o ?g. }
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- NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_assertion type Assertion NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_head.
- NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_assertion wasGeneratedBy ECO_0000203 NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_provenance.
- NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_assertion wasDerivedFrom befree-20150227 NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_provenance.
- NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_assertion SIO_000772 24684794 NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_provenance.
- NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_assertion evidence source_evidence_literature NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_provenance.
- NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_assertion description "[Mutations in the UBQLN2 and SIGMAR1 genes were recently identified in X-linked dominant amyotrophic lateral sclerosis and/or frontotemporal dementia (ALS and/or FTD) and FTD and/or motor neuron disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484436.RAWtgmoxK5_XUXhIwRtemlEkWXF8y6olse_rTDUCS_TE8130_provenance.