Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance.
- NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_assertion description "[The disease is characterized by selective loss of spinal cord motor neurons leading to muscle atrophy and is the result of mutations in the survival motor neuron (SMN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance.
- NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_assertion evidence source_evidence_literature NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance.
- NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_assertion SIO_000772 16108074 NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance.
- NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_assertion wasDerivedFrom befree-20140225 NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance.
- NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_assertion wasGeneratedBy ECO_0000203 NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625790.RAIh4-29tvpt1VNPzSO7SaSMLwi3oANc5rOm242NB4Ih4130_provenance.