Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_assertion> ?p ?o ?g. }
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- NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_assertion type Assertion NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_head.
- NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_assertion wasGeneratedBy ECO_0000218 NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_provenance.
- NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_assertion wasDerivedFrom ctd_human-20150221 NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_provenance.
- NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_assertion SIO_000772 9359047 NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_provenance.
- NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_assertion evidence source_evidence_curated NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_provenance.
- NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_assertion description "[Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13246.RAqlxrz-Q_Fg8OMpwJiUUDnFRrFvLT_J-nLWuBat_8FfU130_provenance.