Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_assertion> ?p ?o ?g. }
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- NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_assertion type Assertion NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_head.
- 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.
- NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_assertion evidence source_evidence_literature NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_provenance.
- NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_assertion SIO_000772 22608501 NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_provenance.
- NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_assertion wasDerivedFrom befree-2016 NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_provenance.
- NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_assertion wasGeneratedBy ECO_0000203 NP983463.RAIc3nTk2pjpCiUWTan7jgYhPA_RH2QvBVdf5Od9Z4NaM130_provenance.