Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance.
- NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_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." NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance.
- NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_assertion evidence source_evidence_literature NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance.
- NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_assertion SIO_000772 23182804 NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance.
- NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_assertion wasDerivedFrom befree-2016 NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance.
- NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_assertion wasGeneratedBy ECO_0000203 NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_provenance.