Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_assertion type Assertion NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_head.
- NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_assertion description "[We identified three distinct heterozygous missense SMAD4 mutations affecting the codon for Ile500 in 11 individuals with Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_provenance.
- NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_assertion evidence source_evidence_curated NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_provenance.
- NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_assertion SIO_000772 22158539 NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_provenance.
- NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_assertion wasDerivedFrom ctd_human-20130708 NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_provenance.
- NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_assertion wasGeneratedBy ECO_0000218 NP30221.RAojeWg9r-gS3CdT6mSczt4w-ZFpb2yKWxme3F3qpDqpc130_provenance.