@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY
> .
@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:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_head
{
this:
np:hasAssertion
dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_assertion
;
np:hasProvenance
dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_provenance
;
np:hasPublicationInfo
dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_assertion
a
np:Assertion
.
dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_provenance
a
np:Provenance
.
dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_assertion
{
miriam-gene:29974
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN623eae6497d0396082d325a7d88965b5
sio:SIO_000628
miriam-gene:29974
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_provenance
{
dgn-np:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_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:NP740021.RAa614jO3_nOhI7FX9WZSbGU0EuktQCToUzmSV6qnk0WY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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" .
}