Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_assertion> ?p ?o ?g. }
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- NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_assertion type Assertion NP433915.RAt0UaHWMYuQPp1P2OARm4MqmUyCR7VxNqTB3vQifpPFY130_head.
- 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.