Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_assertion type Assertion NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_head.
- NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_assertion description "[Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_provenance.
- NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_assertion evidence source_evidence_literature NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_provenance.
- NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_assertion SIO_000772 23182804 NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_provenance.
- NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_assertion wasDerivedFrom befree-2016 NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_provenance.
- NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_assertion wasGeneratedBy ECO_0000203 NP1031272.RAm4yxY66aaCrpBj8OwPqLozobcfMByhvX3d733uLUfy8130_provenance.