@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8
> .
@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:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_head
{
this:
np:hasAssertion
dgn-np:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_assertion
;
np:hasProvenance
dgn-np:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_provenance
;
np:hasPublicationInfo
dgn-np:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_assertion
a
np:Assertion
.
dgn-np:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_provenance
a
np:Provenance
.
dgn-np:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_assertion
{
miriam-gene:434
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN33e646ee144b1c5fcea6851aedf36349
sio:SIO_000628
miriam-gene:434
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_provenance
{
dgn-np:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_assertion
dcterms:description
"[DNA from the French Caucasian population was available for two samples of 100 families with one RA patient and both parents, and for 88 RA index cases from RA ASP families.]. 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:16277672
;
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:NP819618.RAjmo-oIB8A_CTNIxEBI9ltlH__5ojQrdp68X_6bnPra8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:22+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" .
}