Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_assertion> ?p ?o ?g. }
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- NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_assertion type Assertion NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_head.
- NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_assertion description "[The lack of BRCA1 mutations in exon 11 which represents 61% of the entire coding sequence may provide additional insight into BRCA1 associated breast and ovarian tumor development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_provenance.
- NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_assertion evidence source_evidence_literature NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_provenance.
- NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_assertion SIO_000772 9115962 NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_provenance.
- NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_assertion wasDerivedFrom befree-2016 NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_provenance.
- NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_assertion wasGeneratedBy ECO_0000203 NP1371215.RAX4Y1vcS1ziD4sE-kEpSK7rrifTBS0SMJrzqHBMJ2BJA130_provenance.