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- source_evidence_literature type ECO_0000212 NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_provenance.
- NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_assertion description "[An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_provenance.
- NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_assertion evidence source_evidence_literature NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_provenance.
- NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_assertion SIO_000772 17763460 NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_provenance.
- NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_assertion wasDerivedFrom befree-2016 NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_provenance.
- NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_assertion wasGeneratedBy ECO_0000203 NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_provenance.
- befree-2016 importedOn "2016-02-19" NP627694.RAqOIHblp-1pdFEryGSneRfF74N_0O6sZDwuuUQN1HAR0130_provenance.