@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w
> .
@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:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_head
{
this:
np:hasAssertion
dgn-np:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_assertion
;
np:hasProvenance
dgn-np:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_provenance
;
np:hasPublicationInfo
dgn-np:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_assertion
a
np:Assertion
.
dgn-np:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_provenance
a
np:Provenance
.
dgn-np:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_assertion
{
miriam-gene:1280
a
ncit:C16612
.
lld:C0008449
a
ncit:C7057
.
dgn-gda:DGNe447b75bbd1097a7f40a4fd2d90e6acf
sio:SIO_000628
miriam-gene:1280
,
lld:C0008449
;
a
sio:SIO_001121
.
}
dgn-np:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_provenance
{
dgn-np:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_assertion
dcterms:description
"[The involvement of the cartilage specific type II collagen gene (COL2A1) was studied in nine patients with diastrophic dysplasia in the Finnish population, where the prevalence of this chondrodystrophy clearly exceeds that reported for other populations.]. 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:2732992
;
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:NP889516.RAUYDOmFu9EZp3yEt0S4MBCsnrK6ApELWMme4owupe18w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:07+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" .
}