@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y> .
@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:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_head {
  this: np:hasAssertion dgn-np:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_assertion ;
    np:hasProvenance dgn-np:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_assertion a np:Assertion .
  dgn-np:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_provenance a np:Provenance .
  dgn-np:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_assertion {
  miriam-gene:6007 a ncit:C16612 .
  lld:C0036341 a ncit:C7057 .
  dgn-gda:DGNdf35ca8c05eefacda4cbf9c1f06a8605 sio:SIO_000628 miriam-gene:6007 , lld:C0036341 ;
    a sio:SIO_001121 .
}
dgn-np:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_provenance {
  dgn-np:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_assertion dcterms:description "[Evidence is presented that RHD, RHCE, and other RH genes, may be interesting candidates to consider when searching for the genetic basis of hair whorl rotation (i.e., clockwise or counterclockwise), handedness (i.e., right handed, left handed or ambidextrous), speech laterality (i.e., right brained or left brained), speech dyslexia (e.g., stuttering), sexual orientation (i.e., heterosexual, homosexual, bisexual, or transsexual), schizophrenia, bipolar disorder, and autism spectrum disorder.]. 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:16337093 ;
    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:NP505533.RAcjazBjERrwXyXqqGBIRHPytdj86suYRordykYiMGN6Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:01+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" .
}