Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance.
- NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_assertion description "[The combination of developmental and brain imaging features together with mild facial dysmorphism is highly suggestive of this disorder and should prompt subsequent testing of the CASK gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance.
- NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_assertion evidence source_evidence_literature NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance.
- NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_assertion SIO_000772 21954287 NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance.
- NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_assertion wasDerivedFrom befree-20140225 NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance.
- NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_assertion wasGeneratedBy ECO_0000203 NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP872632.RABpWU37Q0pjh9bqhHggNw7fyViSQc-puVo99yNOI0XRw130_provenance.