@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco
> .
@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 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:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_head
{
this:
np:hasAssertion
dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_assertion
;
np:hasProvenance
dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_provenance
;
np:hasPublicationInfo
dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_assertion
a
np:Assertion
.
dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_provenance
a
np:Provenance
.
dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_assertion
{
miriam-gene:1234
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNf8fb45598004608b5176d05887da7637
sio:SIO_000628
miriam-gene:1234
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_provenance
{
dgn-np:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_assertion
dct:description
"[ In a population with a high allelic frequency for the CCR5Delta32 mutation, a significant protection against childhood asthma is evident which is independent of atopy. This protection is lost in the transition between childhood and early adulthood. The contribution of different genetic candidates to the expression of asthma may change with advancing maturity and confound the interpretation of association and linkage studies unless age is taken into account.]. 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:12612298
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47260.RAuU621CHwugec77_7KkowSr8eykvlb1ANVIfQ-xmOwco130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}