@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU
> .
@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:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_head
{
this:
np:hasAssertion
dgn-np:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_assertion
;
np:hasProvenance
dgn-np:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_provenance
;
np:hasPublicationInfo
dgn-np:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_assertion
a
np:Assertion
.
dgn-np:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_provenance
a
np:Provenance
.
dgn-np:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_assertion
{
miriam-gene:1465
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN802c112e975c56fddeb87cb8d93e73ea
sio:SIO_000628
miriam-gene:1465
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_provenance
{
dgn-np:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_assertion
dcterms:description
"[CRP single nucleotide polymorphisms (SNPs) did not increase the risk of asthma, but CRP rs1205 CC genotype significantly decreased the predictive value of forced vital capacity (FVC) in the asthma group (adjusted mean change = -7.54%, 95% CI = -13.82 to -1.25%).]. 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:21790705
;
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:NP751631.RA46XD5cYfxmYm8UsUSlUU8XqeswvSEH58fX3VRzrVVUU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:35+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" .
}