Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_assertion> ?p ?o ?g. }
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- NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_assertion type Assertion NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_head.
- NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_assertion description "[Germline mutations in PTEN can predispose people to Cowden syndrome (CS) and Bannayan-Ruvalcaba-Riley (BRR) syndrome, rare, autosomal dominantly inherited neoplastic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance.
- NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_assertion evidence source_evidence_literature NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance.
- NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_assertion SIO_000772 10807691 NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance.
- NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_assertion wasDerivedFrom befree-2016 NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance.
- NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_assertion wasGeneratedBy ECO_0000203 NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance.