Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance.
- NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_assertion description "[Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance.
- NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_assertion evidence source_evidence_literature NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance.
- NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_assertion SIO_000772 23182804 NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance.
- NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_assertion wasDerivedFrom befree-20140225 NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance.
- NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_assertion wasGeneratedBy ECO_0000203 NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP271851.RAzF46gYR04Kx_5-1csAnjcpp6EeiNU4nbNTCOclyM5G8130_provenance.