Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance.
- NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_assertion description "[The coincidence of chromosome 15 aberrations and beta2-microglobulin gene mutations is causative for the total loss of human leukocyte antigen class I expression in melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance.
- NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_assertion evidence source_evidence_literature NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance.
- NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_assertion SIO_000772 16740750 NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance.
- NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_assertion wasDerivedFrom befree-20140225 NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance.
- NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_assertion wasGeneratedBy ECO_0000203 NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP462369.RAPYqmqfi0XygAjONx1tCgavikdzoBcQvKtfY4STqOtG0130_provenance.