@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I
> .
@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:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_head
{
this:
np:hasAssertion
dgn-np:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_assertion
;
np:hasProvenance
dgn-np:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_provenance
;
np:hasPublicationInfo
dgn-np:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_assertion
a
np:Assertion
.
dgn-np:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_provenance
a
np:Provenance
.
dgn-np:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_assertion
{
miriam-gene:7933
a
ncit:C16612
.
lld:C0729233
a
ncit:C7057
.
dgn-gda:DGN0de9bb6227bfce528b9a8eb4e0ac4c2f
sio:SIO_000628
miriam-gene:7933
,
lld:C0729233
;
a
sio:SIO_001121
.
}
dgn-np:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_provenance
{
dgn-np:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_assertion
dcterms:description
"[However, the IVS20-11delT variant in the NPPS gene and the A861G variant in the leptin receptor gene were more frequent in patients with OPLL in the thoracic spine compared with patients whose OPLL was restricted to the cervical spine.]. 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:15834329
;
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:NP327431.RAfTGLHrhVz5GClHMySR4UvGYgPqn4GvCvKdFSBbh7D9I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}