Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_assertion> ?p ?o ?g. }
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- NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_assertion type Assertion NP1031271.RA3tslArpioQyl6gcuyNaM1xJ3UGyAfV_603BQInQ_hm4130_head.
- 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.