Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance.
- NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_assertion description "[A variant form of hereditary spastic paraplegia & congenital arachnoid cysts has an new autosomal dominant mutation, T614I, in exon 17 of SPG4/may play a role in both focal cortical dysgenesis & corticospinal motoneuron neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance.
- NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_assertion evidence source_evidence_literature NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance.
- NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_assertion SIO_000772 15159500 NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance.
- NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_assertion wasDerivedFrom lhgdn-20090331 NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance.
- NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_assertion wasGeneratedBy ECO_0000203 NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP205146.RAo6_RfprA0ryPKj3e5AYr1fdPu9gA_D1Qu5-2CbB2VAc130_provenance.