Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_assertion> ?p ?o ?g. }
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- NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_assertion type Assertion NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_head.
- NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_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." NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_provenance.
- NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_assertion evidence source_evidence_literature NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_provenance.
- NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_assertion SIO_000772 17903297 NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_provenance.
- NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_assertion wasDerivedFrom gad-20150221 NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_provenance.
- NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_assertion wasGeneratedBy ECO_0000203 NP156713.RAQE7xQRTgC49fgnt4DCmOP66OiJ6RAofuh-v0iFtCGmk130_provenance.