@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc
> .
@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:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_head
{
this:
np:hasAssertion
dgn-np:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_assertion
;
np:hasProvenance
dgn-np:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_provenance
;
np:hasPublicationInfo
dgn-np:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_assertion
a
np:Assertion
.
dgn-np:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_provenance
a
np:Provenance
.
dgn-np:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_assertion
{
miriam-gene:860
a
ncit:C16612
.
lld:C0020725
a
ncit:C7057
.
dgn-gda:DGNb511706bd6b1ff3c3d048a40d7953fa7
sio:SIO_000628
miriam-gene:860
,
lld:C0020725
;
a
sio:SIO_001121
.
}
dgn-np:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_provenance
{
dgn-np:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_assertion
dcterms:description
"[Here we combined shotgun metagenomic and metaproteomic approaches to identify potential functional signatures of CD in stool samples from six twin pairs that were either healthy, or that had CD in the ileum (ICD) or colon (CCD).]. 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:23209564
;
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:NP537392.RASVGL6ISmeC5M3jqroHFDCH4xR3nTFyP_v8_Be_LqYDc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}