Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance.
- NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_assertion description "[Germ line missense mutations in the RET (rearranged during transfection) oncogene are the cause of multiple endocrine neoplasia, type 2 (MEN2), but at present surgery is the only treatment available for MEN2 patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance.
- NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_assertion evidence source_evidence_curated NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance.
- NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_assertion SIO_000772 17664273 NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance.
- NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_assertion wasDerivedFrom ctd_human-20130708 NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance.
- NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_assertion wasGeneratedBy ECO_0000218 NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP28433.RA-HsNzdm1Qv2xFlNsFcydTZkOm98K8QrqcIiqDLd2yKE130_provenance.