Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.
- NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.
- NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_assertion evidence source_evidence_literature NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.
- NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_assertion SIO_000772 18663734 NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.
- NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_assertion wasDerivedFrom befree-20150227 NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.
- NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_assertion wasGeneratedBy ECO_0000203 NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.