@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE
> .
@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:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_head
{
this:
np:hasAssertion
dgn-np:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_assertion
;
np:hasProvenance
dgn-np:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance
;
np:hasPublicationInfo
dgn-np:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_assertion
a
np:Assertion
.
dgn-np:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance
a
np:Provenance
.
dgn-np:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_assertion
{
miriam-gene:7134
a
ncit:C16612
.
lld:C1568272
a
ncit:C7057
.
dgn-gda:DGNdffae5e9929e8181af30167022df4b23
sio:SIO_000628
miriam-gene:7134
,
lld:C1568272
;
a
sio:SIO_001121
.
}
dgn-np:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_provenance
{
dgn-np:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_assertion
dcterms:description
"[The aims of this study were (i) to investigate the association of single nucleotide polymorphisms within the TNC gene, and the additional candidate gene, COL27A1, with AT in two populations, and (ii) to identify if there is a risk haplotype for AT in both populations.]. 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:23192621
;
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:NP525178.RAyfAqWGjLv51nymKfie-X0feXWdeotdiebzH4fEZJHHE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}