@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_head {
  this: np:hasAssertion dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_assertion ;
    np:hasProvenance dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_provenance ;
    np:hasPublicationInfo dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_assertion a np:Assertion .
  dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_provenance a np:Provenance .
  dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_assertion {
  miriam-gene:7871 a ncit:C16612 .
  lld:C0023269 a ncit:C7057 .
  dgn-gda:DGNc4f724d24ce4b12f95cda9ff445444d1 sio:SIO_000628 miriam-gene:7871 , lld:C0023269 ;
    a sio:SIO_001121 .
}
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_provenance {
  dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_assertion dcterms:description "[Group 1 comprises approximately 25% of all LMSs, and is defined by a shared pattern of gene expression, a distinct pattern of genomic changes, and reactivity for at least 3 of 5 immunohistochemistry (IHC) markers (smooth muscle gamma actin, calsequestrin 2, human muscle cofilin2, myosin light chain kinase, and sarcolemmal membrane associated protein), as tested on 271 cases of LMS in tissue microarrays.]. 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:21412072 ;
    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:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:37+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}