Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_assertion> ?p ?o ?g. }
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- NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_assertion type Assertion NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_head.
- NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_assertion description "[The Pro56Ser mutation in the human VAPB MSP domain causes a familial amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_provenance.
- NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_assertion evidence source_evidence_literature NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_provenance.
- NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_assertion SIO_000772 20377183 NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_provenance.
- NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_assertion wasDerivedFrom befree-20140225 NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_provenance.
- NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_assertion wasGeneratedBy ECO_0000203 NP875433.RAPaHRMDxBisIamIzsE14O3FQLePLhBsM9mRKnEXzXJ7I130_provenance.