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- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion type Assertion NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_head.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion wasGeneratedBy ECO_0000218 NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion wasDerivedFrom uniprot-20150221 NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion SIO_000772 11030761 NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion evidence source_evidence_curated NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.