@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I
> .
@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:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_head
{
this:
np:hasAssertion
dgn-np:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_assertion
;
np:hasProvenance
dgn-np:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_provenance
;
np:hasPublicationInfo
dgn-np:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_assertion
a
np:Assertion
.
dgn-np:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_provenance
a
np:Provenance
.
dgn-np:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_assertion
{
miriam-gene:2
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGN94cf0399f2b4b232ae7a8e9a88ae9d03
sio:SIO_000628
miriam-gene:2
,
lld:C0003873
;
a
sio:SIO_001122
.
}
dgn-np:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_provenance
{
dgn-np:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_assertion
dcterms:description
"[ The genetic variation at alpha2m is associated with the severity of RA. Carriers of the alpha2m deletion allele would have increased risk of developing an early active severe form of the disease. Our data suggest that alpha2m could be a valuable target in the treatment of RA.]. 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:11036822
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP49929.RAwO7P_39oVefjhpfnN4mp1iMQRjoCXk9l8NpW9KPqJ3I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}