@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4
> .
@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:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_head
{
this:
np:hasAssertion
dgn-np:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_assertion
;
np:hasProvenance
dgn-np:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_provenance
;
np:hasPublicationInfo
dgn-np:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_assertion
a
np:Assertion
.
dgn-np:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_provenance
a
np:Provenance
.
dgn-np:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_assertion
{
miriam-gene:1280
a
ncit:C16612
.
lld:C2827470
a
ncit:C7057
.
dgn-gda:DGNc7af508d31bd22307a6b76f5dde0d209
sio:SIO_000628
miriam-gene:1280
,
lld:C2827470
;
a
sio:SIO_001121
.
}
dgn-np:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_provenance
{
dgn-np:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_assertion
dcterms:description
"[The etiology of ANFH is unknown, but previous studies have indicated that heritable thrombophilia (increased tendency to form thrombi) and hypofibrinolysis (reduced ability to lyse thrombi), alcohol intake, and steroid use are risk factors for ANFH.]. 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:15179599
;
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:NP697027.RAsHe0zXXsY7mDVKqOJxncD_F8PjOXAMM741SojaYj8s4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}