@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c
> .
@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:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_head
{
this:
np:hasAssertion
dgn-np:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_assertion
;
np:hasProvenance
dgn-np:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_provenance
;
np:hasPublicationInfo
dgn-np:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_assertion
a
np:Assertion
.
dgn-np:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_provenance
a
np:Provenance
.
dgn-np:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_assertion
{
miriam-gene:1673
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNb4a963badd8881f711b76cb2d2af18ab
sio:SIO_000628
miriam-gene:1673
,
lld:C0010674
;
a
sio:SIO_001122
.
}
dgn-np:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_provenance
{
dgn-np:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_assertion
dcterms:description
"[Given the higher complexity found in the genomic organization of the DEFB4 and DEFB104 genes, association studies with CF lung disease severity were performed only for frequent polymorphisms located in DEFB1.]. 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:15820309
;
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:NP60186.RATfls8P3N6w5OYnXeR-BJtCHGyqLdhNcXwFSPObcL91c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}