@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_head
{
this:
np:hasAssertion
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_assertion
;
np:hasProvenance
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_provenance
;
np:hasPublicationInfo
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_assertion
a
np:Assertion
.
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_provenance
a
np:Provenance
.
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNe5bed98dce08056ded7009e3ae049375
sio:SIO_000628
miriam-gene:2837
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_provenance
{
dgn-np:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_assertion
dcterms:description
"[The results show that variation at position 543 in exon 15, which involves substitution of negatively charged aspartic acid (D) by uncharged asparagine (N), and the deletion of TGTG in the 3' UTR may confer protection from development 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:10703607
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP431649.RAcYL2JNpeAzfH3gKk6uiB8Al7ysUt5PffIek1BET7pFE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:51+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}