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- source_evidence_literature type ECO_0000212 NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.
- NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_assertion description "[Taken together, TGFB2 is a rarely mutated gene in patients with syndromic TAAD, and the clinical features of our TGFB2 mutation-positive individuals fit in the scheme of LDS, rather than MFS-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.
- NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_assertion evidence source_evidence_literature NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.
- NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_assertion SIO_000772 24193348 NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.
- NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_assertion wasDerivedFrom befree-20150227 NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.
- NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_assertion wasGeneratedBy ECO_0000203 NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_provenance.