Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance.
- NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_assertion description "[These findings and previous studies have shown that variants within the FUS gene are not a common cause of PD or ET, in comparison to their role in ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance.
- NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_assertion evidence source_evidence_literature NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance.
- NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_assertion SIO_000772 24262168 NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance.
- NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_assertion wasDerivedFrom befree-2016 NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance.
- NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_assertion wasGeneratedBy ECO_0000203 NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1130380.RAXLpY7bEC-JGX3bE_NBaUjCHGMaaKngolNVHRwM__V4I130_provenance.