Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance.
- NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_assertion description "[Herein are illustrated some pitfalls in the diagnosis of melanoma, as well as variants of Spitz's nevus that correlate with specific genomic aberrations such as gains of chromosome 11p and loss of the BAP-1 gene on chromosome 3p.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance.
- NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_assertion evidence source_evidence_literature NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance.
- NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_assertion SIO_000772 22648325 NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance.
- NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_assertion wasDerivedFrom befree-2016 NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance.
- NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_assertion wasGeneratedBy ECO_0000203 NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance.
- befree-2016 importedOn "2016-02-19" NP986096.RAZppEdunadPGgxnZXRuNlhMYGIX0Ux0nH3TEMVAEYlFc130_provenance.