@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ
> .
@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:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_head
{
this:
np:hasAssertion
dgn-np:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_assertion
;
np:hasProvenance
dgn-np:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_assertion
a
np:Assertion
.
dgn-np:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_provenance
a
np:Provenance
.
dgn-np:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_assertion
{
miriam-gene:1234
a
ncit:C16612
.
lld:C0524910
a
ncit:C7057
.
dgn-gda:DGNf78fddf28d5dde4961363bcd8dfe5d98
sio:SIO_000628
miriam-gene:1234
,
lld:C0524910
;
a
sio:SIO_001121
.
}
dgn-np:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_provenance
{
dgn-np:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_assertion
dcterms:description
"[No greater frequency of CCR5-Delta32 homozygosity was seen in an Italian population of patients with chronic hepatitis C. This mutation does not seem to influence either the overall severity of liver disease or the response to viral therapy.]. 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:16721228
;
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:NP715812.RANDyM7LewCIC6eCYuApC5MqMHHPubGRiRYfespihZ6AQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:15+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" .
}