@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w
> .
@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:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_head
{
this:
np:hasAssertion
dgn-np:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_assertion
;
np:hasProvenance
dgn-np:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_provenance
;
np:hasPublicationInfo
dgn-np:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_assertion
a
np:Assertion
.
dgn-np:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_provenance
a
np:Provenance
.
dgn-np:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_assertion
{
miriam-gene:4153
a
ncit:C16612
.
lld:C0003864
a
ncit:C7057
.
dgn-gda:DGNff9e202a090af9a21d55f20d19417432
sio:SIO_000628
miriam-gene:4153
,
lld:C0003864
;
a
sio:SIO_001121
.
}
dgn-np:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_provenance
{
dgn-np:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_assertion
dcterms:description
"[As high levels of MBL and MBL2 associated genotypes have previously been seen to be associated with CRHD, we investigated the association between MBL2 polymorphisms and the presence of acute carditis and arthritis in patients with a history of RF.]. 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:18602696
;
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:NP892767.RAk5F78NMIioXAAWAoY8EmIFxJ0N4HF3_94Le_6tMHB3w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}