Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance.
- NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_assertion description "[We suggest that CADPS2 variants may contribute to ID/ASD development, possibly through a parent-of-origin effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance.
- NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_assertion evidence source_evidence_literature NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance.
- NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_assertion SIO_000772 24737869 NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance.
- NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_assertion wasDerivedFrom befree-20150227 NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance.
- NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_assertion wasGeneratedBy ECO_0000203 NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP253437.RATRH25O0Pp1OPj0fh7bovCR76XWfMGIwKnGi6n1-tYVw130_provenance.