@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk
> .
@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:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_head
{
this:
np:hasAssertion
dgn-np:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_assertion
;
np:hasProvenance
dgn-np:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_provenance
;
np:hasPublicationInfo
dgn-np:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_assertion
a
np:Assertion
.
dgn-np:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_provenance
a
np:Provenance
.
dgn-np:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_assertion
{
miriam-gene:285834
a
ncit:C16612
.
lld:C0033860
a
ncit:C7057
.
dgn-gda:DGN8e54e0e8fc4423ac8e2c6b05b5205c8c
sio:SIO_000628
miriam-gene:285834
,
lld:C0033860
;
a
sio:SIO_001121
.
}
dgn-np:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_provenance
{
dgn-np:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_assertion
dcterms:description
"[Combinatorial analysis of exonic variations in the known genes of the candidate interval revealed that HCG27, PSORS1C3, OTF3, TCF19, HCR, STG, and HCG22 bore no alleles unique to risk haplotypes among the 10 sequenced haplotypes.]. 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:16642438
;
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:NP174839.RAUiLJn9YGCxofdeiW2XKr76cNNNcBtw0fJFcGpHDtoBk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}