Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance.
- NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_assertion description "[We performed a genome-wide scan of two Danish pedigrees with multiple cases of OMM (N = 10) and CMM (N = 3) and other malignancies (with no germline mutations in CDKN2A, CDK4, BRCA1, and BRCA2) to identify melanoma susceptibility genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance.
- NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_assertion evidence source_evidence_literature NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance.
- NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_assertion SIO_000772 16174859 NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance.
- NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_assertion wasDerivedFrom befree-20150227 NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance.
- NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_assertion wasGeneratedBy ECO_0000203 NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP301414.RAcF4FyZ0v39vG3rWlFDsPtardv1DFRNkYINb5-_9Qib0130_provenance.