Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_assertion> ?p ?o ?g. }
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- NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_assertion type Assertion NP340635.RA8gsg64qqiNiyIPX_BpeA_93aLBTFojvwTwWsC_1ext8130_head.
- 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.