Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance.
- 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.
- ctd_human-20150221 importedOn "2015-02-21" NP30436.RA29X-gTidTdlITV-Y2PMKNgYhU6iea0Wtyni1fYDlZEc130_provenance.