Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance.
- NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_assertion description "[The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance.
- NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_assertion evidence source_evidence_literature NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance.
- NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_assertion SIO_000772 24369382 NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance.
- NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_assertion wasDerivedFrom befree-20150227 NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance.
- NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_assertion wasGeneratedBy ECO_0000203 NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP907933.RAa6QIbxvpkeWIc1Q7zFOWSJIEAVhApUiWO9ls6-8VOFA130_provenance.