@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c
> .
@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:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_head
{
this:
np:hasAssertion
dgn-np:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_assertion
;
np:hasProvenance
dgn-np:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_assertion
a
np:Assertion
.
dgn-np:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_provenance
a
np:Provenance
.
dgn-np:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_assertion
{
miriam-gene:356
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGNd55826d34f4e9e2a48edcf5468804a3d
sio:SIO_000628
miriam-gene:356
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_provenance
{
dgn-np:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_assertion
dcterms:description
"[There are many studies performed to assess the associations of CD95 A670G and G1377A polymorphisms with gastric cancer, and the association of CD95L T844C polymorphism with gastric cancer risk, but the data are remaining controversial.]. 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:23681795
;
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:NP904738.RA7u1GMIO9Qn59rkwIWbsW4HU_fGc6UPXJGLZAppF3P-c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}