Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance.
- NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_assertion wasGeneratedBy ECO_0000203 NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance.
- NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_assertion wasDerivedFrom befree-20150227 NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance.
- NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_assertion SIO_000772 17094098 NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance.
- NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_assertion evidence source_evidence_literature NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance.
- NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_assertion description "[Transthyretin amyloid neuropathy of type 1 (Swedish-Portuguese type) is an autosomally inherited progressive disease with a Val30Met mutation, causing generalized sensory-motor polyneuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762011.RANEsF83QX0h003npV4hR0WL5hA5s1K4oas88k8Ekd4kc130_provenance.