Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance.
- NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_assertion description "[Array CGH was used to identify recurrent copy number alterations (RCNA) characteristic of either BRCA1-related or sporadic ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance.
- NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_assertion evidence source_evidence_literature NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance.
- NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_assertion SIO_000772 19802895 NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance.
- NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_assertion wasDerivedFrom befree-20150227 NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance.
- NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_assertion wasGeneratedBy ECO_0000203 NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470396.RAM1dmAef8Zuh4dlnXTYl7mJJg3Q2VU2xSbDzgboTqU3A130_provenance.