Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_assertion> ?p ?o ?g. }
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- NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_assertion type Assertion NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_head.
- NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_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." NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_provenance.
- NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_assertion evidence source_evidence_literature NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_provenance.
- NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_assertion SIO_000772 9736780 NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_provenance.
- NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_assertion wasDerivedFrom befree-20150227 NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_provenance.
- NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_assertion wasGeneratedBy ECO_0000203 NP968041.RAZCrZHfdcg0F0TYHEHbFEsnM0dChv3NPKNKuMDqW3Qh0130_provenance.