Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.