@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg
> .
@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:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_head
{
this:
np:hasAssertion
dgn-np:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_assertion
;
np:hasProvenance
dgn-np:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_provenance
;
np:hasPublicationInfo
dgn-np:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_assertion
a
np:Assertion
.
dgn-np:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_provenance
a
np:Provenance
.
dgn-np:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_assertion
{
miriam-gene:4638
a
ncit:C16612
.
lld:C0036690
a
ncit:C7057
.
dgn-gda:DGN9d7de6f4ec35c343ca35f140b532368b
sio:SIO_000628
miriam-gene:4638
,
lld:C0036690
;
a
sio:SIO_001121
.
}
dgn-np:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_provenance
{
dgn-np:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_assertion
dcterms:description
"[Candidate genes for asthma and allergic diseases co-associated with sepsis including innate immunity receptors and related molecules (CD14, TLR4 and AOAH) and novel genes such as MYLK provide good examples of pleitropic effects of innate immunity genes, where variants conferring risk to specific traits (i.e.]. 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:17989521
;
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:NP262326.RAIgH07QXbf5AtySxh4qPH6alfQQ3mNMaC7O-V939Uilg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}