Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_assertion type Assertion NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_head.
- NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_assertion wasGeneratedBy ECO_0000203 NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_provenance.
- NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_assertion wasDerivedFrom befree-20140225 NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_provenance.
- NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_assertion SIO_000772 17855450 NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_provenance.
- NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_assertion evidence source_evidence_literature NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_provenance.
- NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_assertion description "[Mutations in Alsin are associated with chronic juvenile amyotrophic lateral sclerosis (ALS2), juvenile primary lateral sclerosis and infantile-onset ascending spastic paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP855581.RA2QV87KFZ8ns4hXTtLJ16iSB6XJwo2Q4nS-n2hLHglx4130_provenance.