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- source_evidence_literature type ECO_0000212 NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance.
- NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_assertion description "[Further study of the pathological mechanisms of the mutant forms of seipin may lead to important new insights into motor neuron diseases, including other spastic paraplegia diseases and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance.
- NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_assertion evidence source_evidence_literature NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance.
- NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_assertion SIO_000772 18790819 NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance.
- NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_assertion wasDerivedFrom befree-2016 NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance.
- NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_assertion wasGeneratedBy ECO_0000203 NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance.
- befree-2016 importedOn "2016-02-19" NP692958.RA_fpw_L0QoGulN6qc77pRSWgMVAbzDbFPGboZpJrfOLo130_provenance.