Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance.
- NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_assertion description "[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involve]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance.
- NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_assertion evidence source_evidence_literature NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance.
- NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_assertion SIO_000772 17903297 NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance.
- NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_assertion wasDerivedFrom gad-20150221 NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance.
- NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_assertion wasGeneratedBy ECO_0000203 NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP156700.RAQ2vLFHS9yntRNOS6vqTOKWfIq0z4FMJ1oW25kVv_EZI130_provenance.