Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance.
- NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_assertion description "[Primary structure of an amyloid prealbumin variant in familial polyneuropathy of Jewish origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance.
- NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_assertion evidence source_evidence_literature NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance.
- NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_assertion SIO_000772 6300852 NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance.
- NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_assertion wasDerivedFrom befree-2016 NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance.
- NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_assertion wasGeneratedBy ECO_0000203 NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance.
- befree-2016 importedOn "2016-02-19" NP1305468.RAeZSc8ssCSXXNF3q1gVaHsr4Tc2KmpZJt9-mFEC6dn9A130_provenance.