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- NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_assertion type Assertion NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_head.
- NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_assertion wasGeneratedBy ECO_0000203 NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_provenance.
- NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_assertion wasDerivedFrom befree-20150227 NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_provenance.
- NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_assertion SIO_000772 16791849 NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_provenance.
- NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_assertion evidence source_evidence_literature NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_provenance.
- NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_assertion description "[Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733982.RA4l5Wdnfe43Vnhil_wsGe_ngMP-QnRVQirvtCRh13Wsk130_provenance.