Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_assertion> ?p ?o ?g. }
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- NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_assertion type Assertion NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_head.
- NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_assertion description "[IL17RD mutations were found only in KS individuals and were strongly linked to hearing loss (6/8 individuals).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_provenance.
- NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_assertion evidence source_evidence_literature NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_provenance.
- NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_assertion SIO_000772 23643382 NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_provenance.
- NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_assertion wasDerivedFrom befree-2016 NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_provenance.
- NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_assertion wasGeneratedBy ECO_0000203 NP1074866.RAP3m1mcRM94gR98mOhrScFfINEPSZkehASHzoqJpN9Rs130_provenance.