@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA
> .
@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:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_head
{
this:
np:hasAssertion
dgn-np:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_assertion
;
np:hasProvenance
dgn-np:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_provenance
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np:hasPublicationInfo
dgn-np:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_assertion
a
np:Assertion
.
dgn-np:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_provenance
a
np:Provenance
.
dgn-np:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0271907
a
ncit:C7057
.
dgn-gda:DGN6f075f4f7158deed43d35073a601a739
sio:SIO_000628
miriam-gene:2952
,
lld:C0271907
;
a
sio:SIO_001121
.
}
dgn-np:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_provenance
{
dgn-np:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_assertion
dcterms:description
"[We analyzed the impact of the polymorphisms in CYP4501A1 and GSTM1 and GSTT1 genes on the susceptibility and disease severity in 200 patients with AA and compared the frequency with the normal population.]. 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:16227674
;
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:NP918578.RAUdFncGlJWZzeuu8JEGcm9rTYxjGhY60qte_Q5XKQVfA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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
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"v2.1.0" .
}