@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU
> .
@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:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_head
{
this:
np:hasAssertion
dgn-np:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_assertion
;
np:hasProvenance
dgn-np:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_provenance
;
np:hasPublicationInfo
dgn-np:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_assertion
a
np:Assertion
.
dgn-np:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_provenance
a
np:Provenance
.
dgn-np:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_assertion
{
miriam-gene:7507
a
ncit:C16612
.
lld:C0586407
a
ncit:C7057
.
dgn-gda:DGN7f5ef60077e91cadedf42d5b4d4e83a0
sio:SIO_000628
miriam-gene:7507
,
lld:C0586407
;
a
sio:SIO_001121
.
}
dgn-np:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_provenance
{
dgn-np:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_assertion
dcterms:description
"[Milder skin symptoms in the XPA patients in Tunisia than in those in Japan, despite mostly sunny weather and the unsatisfactory sun protection in Tunisia, should be due to the difference in the mutation site.]. 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:8105686
;
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:NP725622.RAQaA-Q98bG22AEO1CAK_9vuD2IMYP3_ertPUgQCpidQU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}