Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_assertion type Assertion NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_head.
- NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_assertion wasGeneratedBy ECO_0000203 NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_provenance.
- NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_assertion wasDerivedFrom befree-20150227 NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_provenance.
- NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_assertion SIO_000772 9359047 NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_provenance.
- NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_assertion evidence source_evidence_literature NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_provenance.
- NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_assertion description "[Homozygosity for EDN3 mutations has been previously shown to cause the Shah-Waardenburg syndrome, a combination of HSCR with features of the Waardenburg syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP365223.RAj9DfMAKsKqXg_rpRVYCOq2pgOSkzvqwUZQUSqvbixtg130_provenance.