Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance.
- NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_assertion description "[It has been suggested that the C-->T (224Ala-->Val) transition within exon 2 of the cathepsin D gene (CTSD) might represent a risk factor for late onset AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance.
- NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_assertion evidence source_evidence_literature NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance.
- NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_assertion SIO_000772 16543533 NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance.
- NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_assertion wasDerivedFrom befree-20140225 NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance.
- NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_assertion wasGeneratedBy ECO_0000203 NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP175862.RAcQpbslHcU-8jiMTKodw4YT6fqoSnDhHS2w9yAujfFDU130_provenance.