Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_assertion> ?p ?o ?g. }
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- NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_assertion type Assertion NP733419.RAC-oeN_8c4fKVf-CU_-1wOoAbmL7oPEmez2FshVgcXB4130_head.
- 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.