Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance.
- NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_assertion description "[Locus specific probes and CGH confirmed the presence of a ''pure'' partial trisomy 4q due to de novo direct tandem dup(4)(q25q34).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance.
- NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_assertion evidence source_evidence_literature NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance.
- NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_assertion SIO_000772 15581841 NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance.
- NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_assertion wasDerivedFrom befree-20140225 NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance.
- NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_assertion wasGeneratedBy ECO_0000203 NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP493309.RAcUVJ8L4k6YifdxcHG9mLfR36CU-FeeZLhvxEvISAa1Q130_provenance.