Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance.
- NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_assertion description "[Also, the frequencies of DD genotype were significantly increased In HCC group compared to control group and to cirrhosis group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance.
- NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_assertion evidence source_evidence_literature NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance.
- NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_assertion SIO_000772 21925577 NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance.
- NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_assertion wasDerivedFrom befree-2016 NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance.
- NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_assertion wasGeneratedBy ECO_0000203 NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance.
- befree-2016 importedOn "2016-02-19" NP924429.RAlwRee9gdnkX_Kv-Er8DLOsH-XHODVvi4UYPwkh3Lqbs130_provenance.