Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_assertion type Assertion NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_head.
- NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_assertion description "[Expansions of a hexanucleotide repeat (GGGGCC) in the noncoding region of the C9ORF72 gene are the most common cause of the familial form of ALS (C9-ALS), as well as frontotemporal lobar degeneration and other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_provenance.
- NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_assertion evidence source_evidence_literature NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_provenance.
- NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_assertion SIO_000772 24154603 NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_provenance.
- NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_assertion wasDerivedFrom befree-2016 NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_provenance.
- NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_assertion wasGeneratedBy ECO_0000203 NP1122008.RA3wyUuFigGEM6bMmJibNOXkR8qx228cL12lkHb0o9B-8130_provenance.