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- source_evidence_literature type ECO_0000212 NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.
- NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_assertion description "[Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.
- NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_assertion evidence source_evidence_literature NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.
- NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_assertion SIO_000772 20213768 NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.
- NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_assertion wasDerivedFrom befree-2016 NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.
- NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_assertion wasGeneratedBy ECO_0000203 NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.
- befree-2016 importedOn "2016-02-19" NP798696.RAbmHYOLUwT-x-csEVfq9HgCq6KShS9dKuVQ-E4VNE0-k130_provenance.