Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.
- NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_assertion description "[Although APO (a) PNR, APO CI and APO CII genes are analyzed in only few populations, they show a frequency distribution, which is not at variance with that of APO E gene and other widely studied genetic markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.
- NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_assertion evidence source_evidence_literature NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.
- NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_assertion SIO_000772 19014618 NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.
- NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_assertion wasDerivedFrom gad-20130706 NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.
- NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_assertion wasGeneratedBy ECO_0000203 NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.
- gad-20130706 importedOn "2013-07-06" NP65567.RAhWMWYGqhap_-YpNPcZBGhIK9A30W32gsT-FATrAdDio130_provenance.