Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance.
- NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_assertion description "[Heterozygous mutations in GRN are a major cause of frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP), the second most common early-onset dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance.
- NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_assertion evidence source_evidence_literature NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance.
- NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_assertion SIO_000772 22608501 NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance.
- NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_assertion wasDerivedFrom befree-20140225 NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance.
- NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_assertion wasGeneratedBy ECO_0000203 NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_provenance.