@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ
> .
@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:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_head
{
this:
np:hasAssertion
dgn-np:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_assertion
;
np:hasProvenance
dgn-np:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_assertion
a
np:Assertion
.
dgn-np:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_provenance
a
np:Provenance
.
dgn-np:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGNf381836d0037e29b7f2f26438d78ae43
sio:SIO_000628
miriam-gene:3126
,
lld:C0007570
;
a
sio:SIO_001121
.
}
dgn-np:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_provenance
{
dgn-np:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_assertion
dcterms:description
"[Although CD is associated with certain genetic features, carrying the human leukocyte antigen haplotypes DQ2 or DQ8 (a prerequisite for CD development) cannot fully explain who will or who will not develop CD.]. 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:22555186
;
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:NP979495.RAPPci_T73WSkcXdAeYsWfioN7Rw_HMSn82LMdEcw-quQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:08+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" .
}