@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8> .
@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:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_head {
  this: np:hasAssertion dgn-np:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_assertion ;
    np:hasProvenance dgn-np:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_provenance ;
    np:hasPublicationInfo dgn-np:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_assertion a np:Assertion .
  dgn-np:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_provenance a np:Provenance .
  dgn-np:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_assertion {
  miriam-gene:5781 a ncit:C16612 .
  lld:C0034089 a ncit:C7057 .
  dgn-gda:DGNaf1612acb6777ebbb2ae0919b524479b sio:SIO_000628 miriam-gene:5781 , lld:C0034089 ;
    a sio:SIO_001121 .
}
dgn-np:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_provenance {
  dgn-np:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_assertion dcterms:description "[We conclude that (a) most of our clinically diagnosed NS cases were sporadic (b) PTPN11 analysis should be limited to those fulfilling the relevant NS criteria (c) Cardiovascular evaluation should comprise all NS patients, while pulmonary stenosis, short stature, and thorax deformities prevailed among those with PTPN11 mutations.]. 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:21590266 ;
    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:NP703987.RAhXavwndFbOOUdO_XHWHdTFXeNbNDK3HM6ar7M_8KaY8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}