Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_assertion> ?p ?o ?g. }
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- NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_assertion type Assertion NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_head.
- NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_assertion description "[Abnormalities of dystrophin are a common cause of muscular dystrophy and testing for dystrophin gene or protein has become a part of routine diagnostic evaluation of patients who present with progressive proximal muscle weakness, high serum creatine kinase concentrations, and histopathological evidence of a dystrophic process.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_provenance.
- NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_assertion evidence source_evidence_literature NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_provenance.
- NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_assertion SIO_000772 11303236 NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_provenance.
- NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_assertion wasDerivedFrom befree-20150227 NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_provenance.
- NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_assertion wasGeneratedBy ECO_0000203 NP355392.RAbemKPbRL4e5Zi-Je8WW7l_lHcUg-F_oLelmnOj0OslI130_provenance.