@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs
> .
@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:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_head
{
this:
np:hasAssertion
dgn-np:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_assertion
;
np:hasProvenance
dgn-np:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_provenance
;
np:hasPublicationInfo
dgn-np:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_assertion
a
np:Assertion
.
dgn-np:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_provenance
a
np:Provenance
.
dgn-np:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_assertion
{
miriam-gene:788
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNd45887298223464e39089bf9084ae763
sio:SIO_000628
miriam-gene:788
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_provenance
{
dgn-np:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_assertion
dcterms:description
"[Although suggestive signals in AA were apparent at 9p21 and additional CAC and CAD EA loci, overall the data suggest that even larger samples and an ethnic specific focus will be required for GWAS discoveries for CAC in AA 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:23870195
;
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:NP469867.RAHXrsdKhxZu27Kj82FShdja0pRJHoedt2Mzujw0Rlnhs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:41+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" .
}