Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP283604.RABTF1Frop9o4BWPOgbU3yTIqfTzGZ6mqOkPxv1JRj38g130_provenance.