Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance.
- NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_assertion description "[To evaluate the frequency of SQSTM1 mutations, we sequenced this gene in a cohort of patients with FTD or FTD-ALS, with no mutations in known FTD and ALS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance.
- NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_assertion evidence source_evidence_literature NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance.
- NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_assertion SIO_000772 24042580 NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance.
- NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_assertion wasDerivedFrom befree-20150227 NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance.
- NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_assertion wasGeneratedBy ECO_0000203 NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP484453.RAem_idd9XKCoHulg8a6RQUFIE2Wvb0Z9ngis5azD_Y4M130_provenance.