@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg
> .
@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:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_head
{
this:
np:hasAssertion
dgn-np:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_assertion
;
np:hasProvenance
dgn-np:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_provenance
;
np:hasPublicationInfo
dgn-np:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_assertion
a
np:Assertion
.
dgn-np:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_provenance
a
np:Provenance
.
dgn-np:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_assertion
{
miriam-gene:5788
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN92f35cd424c4e63cc6d660edc52ea6ba
sio:SIO_000628
miriam-gene:5788
,
lld:C0026769
;
a
sio:SIO_001122
.
}
dgn-np:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_provenance
{
dgn-np:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_assertion
dcterms:description
"[None of the four newly identified nucleotide substitutions, namely C77T (Pro59Pro) in exon 4, G69C (Asp121His) in exon 5, T127A (Ile187Asn) and A138G (Thr191Ala) in exon 6, was significantly associated to MS.]. 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:12864992
;
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:NP52449.RAwMYd76t04F45M8kArcrg21xr_pFElkzuO5xcRre3Jmg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}