Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance.
- NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_assertion description "[A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance.
- NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_assertion evidence source_evidence_literature NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance.
- NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_assertion SIO_000772 23611888 NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance.
- NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_assertion wasDerivedFrom befree-20150227 NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance.
- NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_assertion wasGeneratedBy ECO_0000203 NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_provenance.