Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance.
- NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_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." NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance.
- NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_assertion evidence source_evidence_literature NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance.
- NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_assertion SIO_000772 9736780 NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance.
- NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_assertion wasDerivedFrom befree-20140225 NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance.
- NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_assertion wasGeneratedBy ECO_0000203 NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP592375.RAD1hkE6JBtyPmW7R0R_oihnpm1Dg_Iv3jkLGV5l2FwEY130_provenance.