@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_head
{
this:
np:hasAssertion
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_assertion
;
np:hasProvenance
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_assertion
a
np:Assertion
.
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_provenance
a
np:Provenance
.
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_assertion
{
miriam-gene:64131
a
ncit:C16612
.
lld:C0750929
a
ncit:C7057
.
dgn-gda:DGN68e45744153a40dafe5ce5aa2488b6c5
sio:SIO_000628
miriam-gene:64131
,
lld:C0750929
;
a
sio:SIO_001121
.
}
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_provenance
{
dgn-np:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_assertion
dcterms:description
"[Several identified eQTLs were novel and these implicate genes involved in bone development (IPO8, XYLT1, and PRKAR1A), and ribosomal pathways related to marrow and bone dysfunction, as potential candidates in the development of CMI.]. 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:25609184
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1257400.RAtWarxRFONbLQZh7F6p419WNU2irTWpBGqWEMLzy9_X0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:16+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}