Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_assertion> ?p ?o ?g. }
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- NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_assertion type Assertion NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_head.
- NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_assertion description "[Given the observed clinical variability of Becker dystrophy, it appears that dystrophin analysis is required for accurately distinguishing between Becker dystrophy and clinically similar autosomal recessive myopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_provenance.
- NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_assertion evidence source_evidence_literature NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_provenance.
- NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_assertion SIO_000772 2668783 NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_provenance.
- NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_assertion wasDerivedFrom befree-2016 NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_provenance.
- NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_assertion wasGeneratedBy ECO_0000203 NP1295806.RA8jhRIkyUSHjwdeC-jq6D7JpnNLA6-FpSSptiR6S9fng130_provenance.