Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance.
- NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_assertion description "[Furthermore, AT-1 defects are a new and important differential diagnosis in patients with low copper and ceruloplasmin in serum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance.
- NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_assertion evidence source_evidence_literature NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance.
- NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_assertion SIO_000772 22243965 NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance.
- NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_assertion wasDerivedFrom befree-20150227 NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance.
- NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_assertion wasGeneratedBy ECO_0000203 NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP323520.RAogvjX5hl7g0cJ4EDX0taA3iaRGrp-CoTJfn9L31eVOQ130_provenance.