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- NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_assertion type Assertion NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_head.
- NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_assertion description "[Through exome sequencing we identified compound heterozygous mutations in WDR19 in a Norwegian family with Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_provenance.
- NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_assertion evidence source_evidence_literature NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_provenance.
- NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_assertion SIO_000772 22019273 NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_provenance.
- NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_assertion wasDerivedFrom befree-20150227 NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_provenance.
- NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_assertion wasGeneratedBy ECO_0000203 NP933093.RAeUMTNB5jA1A9OpkS2K4bm-0_fYwXjILhKEOkA2qUz7I130_provenance.