Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion> ?p ?o ?g. }
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- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion type Assertion NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_head.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion description "[In human muscle, fibrosis is most readily associated with the severe muscle wasting disorder Duchenne muscular dystrophy (DMD), caused by loss of dystrophin gene function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion evidence source_evidence_literature NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion SIO_000772 24877152 NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion wasDerivedFrom befree-20150227 NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.
- NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_assertion wasGeneratedBy ECO_0000203 NP355603.RAIlbDx2CGKuFHnU5ZaBCHp6fDg9icUin4kgpJmYVHDdg130_provenance.