Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance.
- NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_assertion description "[PTEN Hamartoma Tumour Syndrome (PHTS) includes Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome (BRRS), and other conditions resulting from germline mutation of the PTEN tumour suppressor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance.
- NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_assertion evidence source_evidence_literature NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance.
- NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_assertion SIO_000772 21343951 NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance.
- NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_assertion wasDerivedFrom befree-20140225 NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance.
- NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_assertion wasGeneratedBy ECO_0000203 NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP430572.RA6YiHJ6zYnRy0WYo2NoE3G9wwg51EFR2NnPskYSBX6Mc130_provenance.