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- source_evidence_literature type ECO_0000212 NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_provenance.
- NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_assertion description "[Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_provenance.
- NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_assertion evidence source_evidence_literature NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_provenance.
- NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_assertion SIO_000772 20602914 NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_provenance.
- NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_assertion wasDerivedFrom befree-2016 NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_provenance.
- NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_assertion wasGeneratedBy ECO_0000203 NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_provenance.
- befree-2016 importedOn "2016-02-19" NP823698.RAQ0fh1ohp1XtUctJWYWWo1UOYJCEPWZJA_RFDOmT5JsU130_provenance.