Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance.
- NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_assertion description "[Mutations in the X-chromosomal gene (L1CAM) for cell adhesion molecule L1 are associated with a heterogeneous group of conditions that include agenesis of the corpus callosum, hydrocephalus, spastic paraplegia, adducted thumbs and mental retardation (L1-spectrum disease, CRASH or MASA syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance.
- NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_assertion evidence source_evidence_literature NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance.
- NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_assertion SIO_000772 17294222 NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance.
- NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_assertion wasDerivedFrom befree-20140225 NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance.
- NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_assertion wasGeneratedBy ECO_0000203 NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697337.RApbjiNiitQyiRujN2DHCHxTAjGmp-74jClQHx4pdX8Go130_provenance.