Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance.
- NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_assertion description "[Genotypes for ABCA1, IRAK1, and ROS1 may prove useful for assessment of the genetic risk for atherothrombotic cerebral infarction, whereas those for LIMK1 and CYP3A4 may be similarly beneficial in assessment of the genetic risk for intracerebral hemorrhage and subarachnoid hemorrhage, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance.
- NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_assertion evidence source_evidence_literature NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance.
- NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_assertion SIO_000772 18566305 NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance.
- NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_assertion wasDerivedFrom befree-20140225 NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance.
- NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_assertion wasGeneratedBy ECO_0000203 NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance.