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- source_evidence_literature type ECO_0000212 NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_provenance.
- NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_assertion description "[Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_provenance.
- NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_assertion evidence source_evidence_literature NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_provenance.
- NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_assertion SIO_000772 23910792 NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_provenance.
- NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_assertion wasDerivedFrom befree-2016 NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_provenance.
- NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_assertion wasGeneratedBy ECO_0000203 NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1099032.RATR0rhWZCaVPsnALRDLS59SGYNk06dG-76vR3OG86quE130_provenance.