@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8
> .
@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:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_head
{
this:
np:hasAssertion
dgn-np:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_assertion
;
np:hasProvenance
dgn-np:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_provenance
;
np:hasPublicationInfo
dgn-np:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_assertion
a
np:Assertion
.
dgn-np:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_provenance
a
np:Provenance
.
dgn-np:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_assertion
{
miriam-gene:9034
a
ncit:C16612
.
lld:C0033860
a
ncit:C7057
.
dgn-gda:DGNc766c5fd6b3ce74f506a3ff2b0a4bb0a
sio:SIO_000628
miriam-gene:9034
,
lld:C0033860
;
a
sio:SIO_001121
.
}
dgn-np:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_provenance
{
dgn-np:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_assertion
dcterms:description
"[With two rounds of the method and five single nucleotide polymorphisms, molecular haplotypes of 29.3 kb spanning the HCR and CDSN genes, two genes associated with the susceptibility of psoriasis, of 11 members, belonging to a CEPH family, were revealed.]. 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:16134125
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP569189.RA9yEFU5-uM98jNJuZEhCqZRvljIngn6k7tJJaIzSbwx8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}