@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_assertion
;
np:hasProvenance
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_assertion
a
np:Assertion
.
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_provenance
a
np:Provenance
.
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0086543
a
ncit:C7057
.
dgn-gda:DGN3b6abfbd9927da9140c9ec06c4ab4919
sio:SIO_000628
miriam-gene:7515
,
lld:C0086543
;
a
sio:SIO_001121
.
}
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_provenance
{
dgn-np:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_assertion
dcterms:description
"[By using polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP), we analysed XRCC1-Arg399Gln and XPD-Lys751Gln polymorphisms in 195 patients with cataract (75 patients with cortical, 53 with nuclear, 37 with posterior subcapsular, and 30 with mixed type) and in 194 otherwise healthy control group of similar age.]. 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:17637462
;
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:NP273320.RAhXAF6p9v6q2shshKBl2442Kp28wFMzAMVEMfQBNqz2Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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
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dgn-void:disgenetrdf
pav:version
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}