@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw
> .
@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:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_head
{
this:
np:hasAssertion
dgn-np:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_assertion
;
np:hasProvenance
dgn-np:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_provenance
;
np:hasPublicationInfo
dgn-np:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_assertion
a
np:Assertion
.
dgn-np:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_provenance
a
np:Provenance
.
dgn-np:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_assertion
{
miriam-gene:4153
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNcc7b06ba3fb255c476bf041b35b30c25
sio:SIO_000628
miriam-gene:4153
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_provenance
{
dgn-np:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_assertion
dcterms:description
"[To determine whether variant alleles of the mannose binding lectin (MBL) gene causing low serum concentrations of MBL are associated with increased susceptibility to rheumatoid arthritis (RA) and erosive outcome in an inception cohort of patients with early polyarthritis.]. 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:11361219
;
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:NP252067.RATsP1r1oz9znhtuDret9hTYoRv-U6MPc2XADsxZlgqWw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:21+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" .
}