Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance.
- NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_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." NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance.
- NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_assertion evidence source_evidence_literature NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance.
- NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_assertion SIO_000772 16174859 NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance.
- NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_assertion wasDerivedFrom befree-20140225 NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance.
- NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_assertion wasGeneratedBy ECO_0000203 NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP207044.RAEXhHTUAfY0hOM0cidTp_mRzfzJ3Nymp2SPGbpW16GjQ130_provenance.