Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance.
- NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_assertion wasGeneratedBy ECO_0000203 NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance.
- NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_assertion wasDerivedFrom befree-20140225 NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance.
- NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_assertion SIO_000772 19793054 NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance.
- NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_assertion evidence source_evidence_literature NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance.
- NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_assertion description "[Presence of the MDCR is associated with a mild phenotype, including growth delay (GD), mental retardation (MR), seizures, cafè au lait skin (CALS) spots and minor facial dysmorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP173739.RAQMNlxQ6jf_m46CffuQ8bn4SjgVvN-JeK_m4Ll3M2gUs130_provenance.