Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_assertion> ?p ?o ?g. }
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- NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_assertion type Assertion NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_head.
- NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_assertion description "[Substantial efforts have been deployed in the past decade to identify the genetic causes of amyotrophic lateral sclerosis (ALS), and we hypothesized here that mutations in SORT1 or aberrant SORT1 splicing reduce progranulin level and promote neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_provenance.
- NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_assertion evidence source_evidence_literature NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_provenance.
- NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_assertion SIO_000772 22361451 NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_provenance.
- NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_assertion wasDerivedFrom befree-20150227 NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_provenance.
- NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_assertion wasGeneratedBy ECO_0000203 NP433935.RA1ZBzcxO_URUU4DP1gwH3hDr6YxRdncUdS8FFoA6jJAs130_provenance.