Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance.
- NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_assertion description "[No significant associations were found. Within the limitations imposed by the size of the clinical sample, these findings suggest that the above polymorphic loci do not contribute significantly to risk for TD. Further examination of loci that yielded posi]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance.
- NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_assertion evidence source_evidence_literature NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance.
- NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_assertion SIO_000772 14583797 NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance.
- NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_assertion wasDerivedFrom gad-20150221 NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance.
- NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_assertion wasGeneratedBy ECO_0000203 NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP63893.RAZ2wPJd3OUn5bPqhMYN3p3Qk16fy83F1xBKgvxtRj2D8130_provenance.