Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_assertion> ?p ?o ?g. }
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- NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_assertion type Assertion NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_head.
- NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_assertion description "[Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance.
- NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_assertion evidence source_evidence_curated NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance.
- NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_assertion SIO_000772 22158539 NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance.
- NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_assertion wasDerivedFrom ctd_human-20150221 NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance.
- NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_assertion wasGeneratedBy ECO_0000218 NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance.