Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance.
- NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_assertion description "[TGFBR2 and TGFBR1 mutations were identified in a subset of patients with MFS (MFS2, OMIM #154705) and other MFS-related disorders, including Loeys-Dietz syndrome (LDS, #OMIM 609192) and familial thoracic aortic aneurysms and dissections (TAAD2, #OMIM 608987).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance.
- NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_assertion evidence source_evidence_literature NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance.
- NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_assertion SIO_000772 17061023 NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance.
- NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_assertion wasDerivedFrom befree-20140225 NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance.
- NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_assertion wasGeneratedBy ECO_0000203 NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP424843.RAjNUV4fFTVZuk4dr_s1gs-6dpWwmPZLTw9F_zsvbwUiE130_provenance.