Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance.
- NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_assertion description "[L1CAM, therefore, harbours mutations leading to either MASA syndrome or HSAS, and might be frequently implicated in X-linked mental retardation with or without hydrocephalus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance.
- NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_assertion evidence source_evidence_literature NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance.
- NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_assertion SIO_000772 7920660 NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance.
- NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_assertion wasDerivedFrom befree-20140225 NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance.
- NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_assertion wasGeneratedBy ECO_0000203 NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP191414.RAUCzZQHnan60nr5CaCLL12c3HgtYUpJBixddHlZn8uk8130_provenance.