Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_assertion type Assertion NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_head.
- NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_assertion description "[Autosomal dominant familial spastic paraplegia (FSP) is a genetically heterogeneous neurodegenerative disorder displaying anticipation for which three loci have been mapped to the chromosomal positions 14q11.2-q24.3 (SPG3), 2p21-p24 (SPG4) and 15q11.1 (SPG6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_provenance.
- NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_assertion evidence source_evidence_literature NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_provenance.
- NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_assertion SIO_000772 9736780 NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_provenance.
- NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_assertion wasDerivedFrom befree-2016 NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_provenance.
- NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_assertion wasGeneratedBy ECO_0000203 NP1403914.RA_jnBJ65gZVXWg5sSCjMMV3fJRTz_oaP9o6obYtDlxWk130_provenance.