Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance.
- NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_assertion description "[In this proteins two amino acid polymorphisms (Ile/Val A-- > G) have been associated with an increased risk for Alzheimer's disease (AD) and the combination with CTSD-T allele seems to increase this risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance.
- NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_assertion evidence source_evidence_literature NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance.
- NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_assertion SIO_000772 16784755 NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance.
- NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_assertion wasDerivedFrom lhgdn-20090331 NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance.
- NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_assertion wasGeneratedBy ECO_0000203 NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP173721.RA8N8SEQ851BPZLuS4ifzexegFF-W1GgS3orMhbpZ-2-Y130_provenance.