Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance.
- NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_assertion description "[A microdissection-based approach was used to analyse 30 archived primary cutaneous melanomas and associated naevi for loss of heterozygosity (LOH) at 9p21 using the polymorphic DNA markers D9S171 and IFNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance.
- NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_assertion evidence source_evidence_literature NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance.
- NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_assertion SIO_000772 12690309 NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance.
- NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_assertion wasDerivedFrom befree-20140225 NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance.
- NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_assertion wasGeneratedBy ECO_0000203 NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP620904.RAKbNt0GrjsEpssMYN_CLAFCe1YX6xmKPRE3_NS8M3dfw130_provenance.