Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_assertion> ?p ?o ?g. }
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- NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_assertion type Assertion NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_head.
- NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_assertion description "[Multiple DGC cases in a family, DGC at a young age in an individual or the combination of DGC andlobular breast cancer (LBC) in an individual or a family define the hereditary DGC syndrome (HDGC), and testing for germline CDH1 mutations is warranted in HDGC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_provenance.
- NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_assertion evidence source_evidence_literature NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_provenance.
- NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_assertion SIO_000772 23709761 NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_provenance.
- NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_assertion wasDerivedFrom befree-20140225 NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_provenance.
- NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_assertion wasGeneratedBy ECO_0000203 NP932643.RAUyzoIANS8Blp-inF1xeRKaXLs1XaTK8lK2oE0d-x06w130_provenance.