@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0
> .
@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:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_head
{
this:
np:hasAssertion
dgn-np:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_assertion
;
np:hasProvenance
dgn-np:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_provenance
;
np:hasPublicationInfo
dgn-np:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_assertion
a
np:Assertion
.
dgn-np:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_provenance
a
np:Provenance
.
dgn-np:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_assertion
{
miriam-gene:720
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN4f661823d5527281734f2c0181a0d2e6
sio:SIO_000628
miriam-gene:720
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_provenance
{
dgn-np:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_assertion
dcterms:description
"[Since autism has several autoimmune features, the frequencies of null (no protein produced) alleles at the C4A and C4B loci were studied in 19 subjects with autism and their family members.]. 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:2004485
;
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:NP917983.RAS_WukbJKNBrOmX2mNRTC2K4McQcrx7NNy-P9RmeHRg0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}