@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE
> .
@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:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_head
{
this:
np:hasAssertion
dgn-np:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_assertion
;
np:hasProvenance
dgn-np:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_provenance
;
np:hasPublicationInfo
dgn-np:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_assertion
a
np:Assertion
.
dgn-np:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_provenance
a
np:Provenance
.
dgn-np:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNb4e202c2b26fd96b715cfe94d4488390
sio:SIO_000628
miriam-gene:367
,
lld:C0004352
;
a
sio:SIO_001122
.
}
dgn-np:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_provenance
{
dgn-np:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_assertion
dcterms:description
"[The results lend some support for an influence of the studied polymorphisms on the susceptibility for autism, but argue against the possibility that mutations in the AR gene are common in subjects with this condition.]. 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:19167832
;
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:NP96066.RAQWSnClxOo7SEI9I2AW6qfRpjrm8G_vKgqcAFXVaCCRE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:33+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" .
}