Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_assertion> ?p ?o ?g. }
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- NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_assertion type Assertion NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_head.
- NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_assertion description "[A hexanucleotide repeat expansion in C9ORF72 causes chromosome 9p linked FTLD/ALS and is the most common cause of familial ALS accounting for about 40 % of familial cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_provenance.
- NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_assertion evidence source_evidence_literature NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_provenance.
- NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_assertion SIO_000772 22477152 NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_provenance.
- NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_assertion wasDerivedFrom befree-20140225 NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_provenance.
- NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_assertion wasGeneratedBy ECO_0000203 NP514412.RA_LepmVyeZhBYAEiPJMNNy5FnbEqncWgkPRV1J_JV89o130_provenance.