Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance.
- NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_assertion description "[We have explored the application of array-CGH to the detection of such changes on a set of 20 samples consisting of patients with eye diseases associated with changes on chromosome 6p25 together with unaffected individuals, as well as two samples from tuberous sclerosis 2 (TSC2)-affected patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance.
- NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_assertion evidence source_evidence_literature NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance.
- NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_assertion SIO_000772 15221791 NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance.
- NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_assertion wasDerivedFrom befree-2016 NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance.
- NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_assertion wasGeneratedBy ECO_0000203 NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance.
- befree-2016 importedOn "2016-02-19" NP450002.RAWFAvi6ECs76vrGBa3kcKPKtOo_OrNI6kvF7DZX9_PI4130_provenance.