@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0
> .
@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:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_head
{
this:
np:hasAssertion
dgn-np:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_assertion
;
np:hasProvenance
dgn-np:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_provenance
;
np:hasPublicationInfo
dgn-np:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_assertion
a
np:Assertion
.
dgn-np:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_provenance
a
np:Provenance
.
dgn-np:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_assertion
{
miriam-gene:23677
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN2c3e49bea9aed99d07e8ebb8279b0fb0
sio:SIO_000628
miriam-gene:23677
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_provenance
{
dgn-np:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_assertion
dcterms:description
"[We searched for polymorphisms in the human TTP gene and for this purpose, we sequenced the entire TTP gene in 20 Japanese individuals (ten with RA and ten healthy volunteers) and found one single nucleotide polymorphism (SNP) in the promoter region.]. 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:18536977
;
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:NP864866.RAa8gTRkJRvEs6PKgYIVIx6ZtVr3OjdqX4_MsPArAhRC0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:48+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" .
}