Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_assertion type Assertion NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_head.
- NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_assertion description "[We suggest that EXOSC3 mutations may present not only as pontocerebellar hypoplasia type 1, but also as a complicated form of hereditary spastic paraplegia without pontine hypoplasia or atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.
- NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_assertion evidence source_evidence_literature NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.
- NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_assertion SIO_000772 25149867 NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.
- NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_assertion wasDerivedFrom befree-2016 NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.
- NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_assertion wasGeneratedBy ECO_0000203 NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.