@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g
> .
@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:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_head
{
this:
np:hasAssertion
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_assertion
;
np:hasProvenance
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_provenance
;
np:hasPublicationInfo
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_assertion
a
np:Assertion
.
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_provenance
a
np:Provenance
.
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_assertion
{
miriam-gene:450095
a
ncit:C16612
.
lld:C0036202
a
ncit:C7057
.
dgn-gda:DGNcc43b56d758d7ef034179d9e45180a5c
sio:SIO_000628
miriam-gene:450095
,
lld:C0036202
;
a
sio:SIO_001121
.
}
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_provenance
{
dgn-np:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_assertion
dcterms:description
"[However, our study identified the allele TNFB*1, detected by the presence of a NCO: I restriction site, as a marker of prolonged clinical course, with the resolution of sarcoidosis being defined as the disappearance of all clinical symptoms, physical signs of active lesions, abnormal chest radiograph findings, and abnormal results of pulmonary function and biochemical tests.]. 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:11243953
;
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:NP449856.RAXSDc-iMubCD8UsQghxrEOtsIaTl4F6Rr5gfq5Apjr2g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}