Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_assertion> ?p ?o ?g. }
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- NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_assertion type Assertion NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_head.
- NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_assertion description "[Mutations in UBQLN2 encoding ubiquilin-2 have recently been identified in families with dominant X-linked juvenile and adult-onset amyotrophic lateral sclerosis (ALS) and ALS/dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_provenance.
- NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_assertion evidence source_evidence_literature NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_provenance.
- NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_assertion SIO_000772 22169395 NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_provenance.
- NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_assertion wasDerivedFrom befree-20140225 NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_provenance.
- NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_assertion wasGeneratedBy ECO_0000203 NP591894.RAyrmyH0FQiiG2YzW7X072ZSFbrOjbFr5fbBqFPp3E1T8130_provenance.