@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM
> .
@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/v4.0.0/void/
> .
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_head
{
this:
np:hasAssertion
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_assertion
;
np:hasProvenance
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_provenance
;
np:hasPublicationInfo
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_assertion
a
np:Assertion
.
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_provenance
a
np:Provenance
.
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0026269
a
ncit:C7057
.
dgn-gda:DGNfad40423c09cc4daf2bc00f8724d1a08
sio:SIO_000628
miriam-gene:3077
,
lld:C0026269
;
a
sio:SIO_001121
.
}
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_provenance
{
dgn-np:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_assertion
dcterms:description
"[Genotyping the two sets of MS patients (112 benign and 51 malignant) provided no evidence to suggest that mutations in HFE have any outcome modifying activity, although small effects cannot be ruled out.]. 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:18675463
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP685648.RAqU9469p4HZwjgA2m87Gr6LV48CPzKttPoAOaIxlqxfM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:56+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}