@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0
> .
@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:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_head
{
this:
np:hasAssertion
dgn-np:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_assertion
;
np:hasProvenance
dgn-np:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_provenance
;
np:hasPublicationInfo
dgn-np:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_assertion
a
np:Assertion
.
dgn-np:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_provenance
a
np:Provenance
.
dgn-np:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0398623
a
ncit:C7057
.
dgn-gda:DGN95ed49407495d7ace8b52fe420460e91
sio:SIO_000628
miriam-gene:4846
,
lld:C0398623
;
a
sio:SIO_001121
.
}
dgn-np:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_provenance
{
dgn-np:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_assertion
dcterms:description
"[Limited by the small numbers of patients with multifocal osteonecrosis, this exploratory study suggested that thrombophilia was associated with both idiopathic multifocal osteonecrosis and secondary multifocal osteonecrosis, as was the eNOS T-786C polymorphism.]. 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:18829920
;
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:NP389358.RAPPaQ4Ln4ojNQRWHRXZ-DI5HfQl4QyGWJlJc3VAXg4Y0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}