@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_head { this: np:hasAssertion dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_assertion; np:hasProvenance dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_provenance; np:hasPublicationInfo dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_publicationInfo; a np:Nanopublication . dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_assertion a np:Assertion . dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_provenance a np:Provenance . dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_publicationInfo a np:PublicationInfo . } dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_assertion { miriam-gene:1756 a ncit:C16612 . lld:C0751336 a ncit:C7057 . dgn-gda:DGN903d88d539ec2e88a0e064c6c06728e3 sio:SIO_000628 miriam-gene:1756, lld:C0751336; a sio:SIO_001121 . } dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_provenance { dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_assertion dcterms:description "[The spectacular progress concerning dystrophin and its pathology, the dystrophinopathies, has led to a somewhat arbitrarily separated heterogeneous group of nondystrophinopathic muscular dystrophies that currently comprise the Emery-Dreifuss type, the nosologically heterogeneous autosomal-recessive limb-girdle muscular dystrophy, the severe childhood autosomal-recessive muscular dystrophy, the merosin-positive and -negative congenital muscular dystrophies, the autosomal-recessive distal muscular dystrophy of Miyoshi, the facio-scapulo-humeral muscular dystrophy, and myotonic dystrophy, both the adult and neonatal variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:8795845; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP658085.RAI7hMjZSCt-XipA3En15B-4pqYxMtv1Dr0MjqbEvGyeo130_publicationInfo { this: dcterms:created "2014-10-02T12:38:36+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }