@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk> .
@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:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_head {
  this: np:hasAssertion dgn-np:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_assertion ;
    np:hasProvenance dgn-np:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_provenance ;
    np:hasPublicationInfo dgn-np:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_assertion a np:Assertion .
  dgn-np:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_provenance a np:Provenance .
  dgn-np:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_assertion {
  miriam-gene:2693 a ncit:C16612 .
  lld:C0013336 a ncit:C7057 .
  dgn-gda:DGN45213d27f3906a045bb701fab984d9ef sio:SIO_000628 miriam-gene:2693 , lld:C0013336 ;
    a sio:SIO_001121 .
}
dgn-np:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_provenance {
  dgn-np:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_assertion dcterms:description "[Pedigree analysis revealed an accumulation of the history of short stature in father's relatives, although there was no consanguinity.We performed sequencing analysis of GH1 and GHSR gene in the siblings.We detected SNPs in the GH1 gene in the combination of the - 278G, - 57T, +1169T, and +2103C in one allele from the father and the - 278T, - 57G, +1169 A, and +2103T in the other allele from the mother in the siblings.]. 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:22549341 ;
    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:NP353944.RAMRRDYIFNLJTZWXR3e7YZq9CkZasIQN9TFUr3DWT62Hk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:27+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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> ;
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