Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_assertion> ?p ?o ?g. }
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- NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_assertion type Assertion NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_head.
- NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_assertion description "[We determined the prevalence of SCA2 and SCA3 mutations in a cohort of ET and atypical Parkinsonism patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_provenance.
- NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_assertion evidence source_evidence_literature NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_provenance.
- NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_assertion SIO_000772 17712857 NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_provenance.
- NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_assertion wasDerivedFrom lhgdn-20090331 NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_provenance.
- NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_assertion wasGeneratedBy ECO_0000203 NP174218.RAFJ9N9qbWJD_oRRMf6yRaUG22N0QXs1M06Hlp0jm0WbU130_provenance.