Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.
- NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_assertion description "[Further studies are needed to explore contributions from other genetic factors such as rare variants in these genes and variation outside of these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.
- NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_assertion evidence source_evidence_literature NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.
- NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_assertion SIO_000772 20810604 NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.
- NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_assertion wasDerivedFrom gad-20130706 NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.
- NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_assertion wasGeneratedBy ECO_0000203 NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.
- gad-20130706 importedOn "2013-07-06" NP51053.RAoX6pJgCnlPP9RAqsV8fcIbodQoRmHAIX_kI8AGt5mEk130_provenance.