Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_assertion> ?p ?o ?g. }
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- NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_assertion type Assertion NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_head.
- NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_assertion description "[Loss of CSTB function due to mutations is consistent with the observed neurodegenerative pathology and phenotype, but the functional link to the epileptic phenotype of EPM1 remains largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_provenance.
- NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_assertion evidence source_evidence_literature NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_provenance.
- NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_assertion SIO_000772 14526183 NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_provenance.
- NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_assertion wasDerivedFrom befree-20140225 NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_provenance.
- NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_assertion wasGeneratedBy ECO_0000203 NP814414.RAlNrAOVXGH7Es7XNT_nvFCa_tIfV2PZMTjHXPpzTIpAA130_provenance.