Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance.
- NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_assertion description "[In hereditary cystatin C amyloid angiopathy (HCCAA), presence of the Leu68 --> Gln substitution in cystatin C is coupled to a decreased concentration of this major cysteine proteinase inhibitor in cerebrospinal fluid and leads to its amyloid deposition in the brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance.
- NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_assertion evidence source_evidence_literature NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance.
- NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_assertion SIO_000772 9860845 NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance.
- NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_assertion wasDerivedFrom befree-20150227 NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance.
- NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_assertion wasGeneratedBy ECO_0000203 NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333657.RAVwYMqEEENIbTEUo735WQwu4KQTr_91a_C-a9SwFaAgo130_provenance.