@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8
> .
@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:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_head
{
this:
np:hasAssertion
dgn-np:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_assertion
;
np:hasProvenance
dgn-np:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_provenance
;
np:hasPublicationInfo
dgn-np:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_assertion
a
np:Assertion
.
dgn-np:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_provenance
a
np:Provenance
.
dgn-np:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_assertion
{
miriam-gene:23705
a
ncit:C16612
.
lld:C0021290
a
ncit:C7057
.
dgn-gda:DGN65f470bdea9e4fb27295fd2037d63277
sio:SIO_000628
miriam-gene:23705
,
lld:C0021290
;
a
sio:SIO_001121
.
}
dgn-np:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_provenance
{
dgn-np:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_assertion
dcterms:description
"[However, the homogeneous human sequence type 17 (ST-17) complex, known to be significantly associated with invasive neonatal disease, was the only human lineage found to be clustered within the bovine population and was distinct from all the other human lineages.]. 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:15131184
;
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:NP776450.RAEI7veywyEZBuuOEDdXdQDMmDWmJ755e-H-DnlBXVKH8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:50+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" .
}