Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_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." NP623456.RACKURcCWx8CFyGvewvDftvRrCEW82YVlQ82QxgG9gkx4130_provenance.
- 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." provenance.
- 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." provenance.
- 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." provenance.
- 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." 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.
- NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_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." NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_provenance.
- NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_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." NP434140.RAsTWGYaq_UtpcDpmgNVtKOLCI75In8yDqMDovNyTU6x0130_provenance.
- NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_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." NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_provenance.
- NP983464.RAFSOiGrIdp01Hcb-KrAgXLzfcMcmN4v1roqHPck3xFIg130_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." NP983464.RAFSOiGrIdp01Hcb-KrAgXLzfcMcmN4v1roqHPck3xFIg130_provenance.
- NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_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." NP983465.RAEvRN5zO7UH0GpHeSmJxjRd73OdCgCHp_dueac5LCNY0130_provenance.
- NP983462.RA1DmSQbzoZUaSU-AJ_acLpcpJmWrL7mDCkDknpz8v1Wg130_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." NP983462.RA1DmSQbzoZUaSU-AJ_acLpcpJmWrL7mDCkDknpz8v1Wg130_provenance.