@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4
> .
@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:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_head
{
this:
np:hasAssertion
dgn-np:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_assertion
;
np:hasProvenance
dgn-np:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_provenance
;
np:hasPublicationInfo
dgn-np:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_assertion
a
np:Assertion
.
dgn-np:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_provenance
a
np:Provenance
.
dgn-np:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN2cf680beee815816ec224149c114e8f3
sio:SIO_000628
miriam-gene:7450
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_provenance
{
dgn-np:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_assertion
dcterms:description
"[In summary, vWF gene polymorphisms at site A1381T were not associated with coronary heart disease, but plasma vWF levels were influenced by vWF gene polymorphisms at site A1381T, blood type and coronary heart disease.]. 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:22923007
;
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:NP179041.RAxXzNm634lPUbhnd97cN1YUxvYKw_ZvrSgJJDlHhCWU4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}