Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_assertion> ?p ?o ?g. }
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- NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_assertion type Assertion NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_head.
- NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_assertion description "[A number of human genetic disorders have been mapped to the region where STK9 has been localized including Nance-Horan (NH) syndrome, oral-facial-digital syndrome type 1 (OFD1), and a novel locus for nonsyndromic sensorineural deafness (DFN6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_provenance.
- NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_assertion evidence source_evidence_literature NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_provenance.
- NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_assertion SIO_000772 9721213 NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_provenance.
- NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_assertion wasDerivedFrom befree-20150227 NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_provenance.
- NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_assertion wasGeneratedBy ECO_0000203 NP719405.RAYRmN2Iq-paQ65IGzexyCW9l0zGGQXkhbLhGdsfPhrcQ130_provenance.