@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I
> .
@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/v3.0.0/void/
> .
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_head
{
this:
np:hasAssertion
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_assertion
;
np:hasProvenance
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_provenance
;
np:hasPublicationInfo
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_assertion
a
np:Assertion
.
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_provenance
a
np:Provenance
.
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_assertion
{
miriam-gene:404672
a
ncit:C16612
.
lld:C0043346
a
ncit:C7057
.
dgn-gda:DGN7f3cbc4be47f750fbecef0d249ee5107
sio:SIO_000628
miriam-gene:404672
,
lld:C0043346
;
a
sio:SIO_001121
.
}
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_provenance
{
dgn-np:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_assertion
dcterms:description
"[There are several hereditary diseases which are known to go along with genetic defects of DNA repair mechanisms comprising Xeroderma pigmentosum (XP), Cockayne syndrome (CS), Trichothiodystrophy (TTD), Werner syndrome (WS), Bloom syndrome (BS), Fanconi anemia (FA) and Ataxia telangiectasia (AT).]. 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:23522627
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP992109.RA1qZmWvp9JmXO7B5i23A-FjY1w3BURrojGqqR4rKnf-I130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:49+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}