Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_assertion> ?p ?o ?g. }
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- NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_assertion type Assertion NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_head.
- NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_assertion description "[The discovery of multiple tau gene mutations that are pathogenic for hereditary frontotemporal dementia and parkinsonism linked to chromosome 17 in many kindreds, as well as the demonstration that tau polymorphisms are genetic risk factors for sporadic tauopathies, directly implicate tau abnormalities in the onset/progression of neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_provenance.
- NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_assertion evidence source_evidence_literature NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_provenance.
- NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_assertion SIO_000772 11207421 NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_provenance.
- NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_assertion wasDerivedFrom befree-2016 NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_provenance.
- NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_assertion wasGeneratedBy ECO_0000203 NP308557.RASBiCfLTltjq268QSZNhq14nq5wvm_8KbyeRDIoN_eqE130_provenance.