@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_head
{
this:
np:hasAssertion
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_assertion
;
np:hasProvenance
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_provenance
;
np:hasPublicationInfo
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_assertion
a
np:Assertion
.
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_provenance
a
np:Provenance
.
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_assertion
{
miriam-gene:2328
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN685ce21ae2b45696e8dab1ec63c939be
sio:SIO_000628
miriam-gene:2328
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_provenance
{
dgn-np:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_assertion
dcterms:description
"[tatistically significant heterogeneity in the relative frequencies of single and multiple site alleles, haplotypes, and genotypes of the human FMO3 among ethnic subdivisions suggests that population differences in the susceptibility of humans to abnormal ]. 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:11717182
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP52089.RA8jaujsyAnfGOR5t9vG4vZ3jQHb_eAIzQ4Bo796a8sZc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:08+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}