Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance.
- befree-2016 importedOn "2016-02-19" NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance.
- NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_assertion wasGeneratedBy ECO_0000203 NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance.
- NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_assertion wasDerivedFrom befree-2016 NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance.
- NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_assertion SIO_000772 2574869 NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance.
- NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_assertion evidence source_evidence_literature NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance.
- NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_assertion description "[Using a full length cystatin C cDNA probe and the Alu I restriction enzyme a total of 33 patients with senile dementia, Alzheimer type and 31 Down's syndrome patients have been investigated for the presence of the 630 bp Alu I restriction fragment length polymorphism in the cystatin C gene detected in Icelandic patients with hereditary cystatin C amyloid angiopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1269304.RA42HHf_XS5KTUqbvTJGmh30ekW8wljLD8F5aNxwm2sks130_provenance.