@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U
> .
@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:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_head
{
this:
np:hasAssertion
dgn-np:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_assertion
;
np:hasProvenance
dgn-np:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_provenance
;
np:hasPublicationInfo
dgn-np:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_assertion
a
np:Assertion
.
dgn-np:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_provenance
a
np:Provenance
.
dgn-np:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_assertion
{
miriam-gene:6439
a
ncit:C16612
.
lld:C0024117
a
ncit:C7057
.
dgn-gda:DGN2e913377a83e56506e7883a83bfc4983
sio:SIO_000628
miriam-gene:6439
,
lld:C0024117
;
a
sio:SIO_001121
.
}
dgn-np:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_provenance
{
dgn-np:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_assertion
dcterms:description
"[In participants with severe COPD, SNPs in EPHX1 and SERPINE2 were associated with hypoxemia in two separate study populations, and SNPs from SFTPB were associated with pulmonary artery pressure in the NETT participants.]. 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:19017876
;
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:NP597352.RAWqjtFHWWb9dM4Md4sib2zghciRc1qVTNbkSCW9W5Q_U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}