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- NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_assertion type Assertion NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_head.
- 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.
- NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_assertion evidence source_evidence_literature NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_provenance.
- NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_assertion SIO_000772 22608501 NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_provenance.
- NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_assertion wasDerivedFrom befree-20150227 NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_provenance.
- NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_assertion wasGeneratedBy ECO_0000203 NP433983.RAowfiAbapOfnUpxzerCBu0z8wJau9Y8OPQUAzDMeQbhU130_provenance.