@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs
> .
@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:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_head
{
this:
np:hasAssertion
dgn-np:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_assertion
;
np:hasProvenance
dgn-np:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_provenance
;
np:hasPublicationInfo
dgn-np:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_assertion
a
np:Assertion
.
dgn-np:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_provenance
a
np:Provenance
.
dgn-np:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_assertion
{
miriam-gene:27102
a
ncit:C16612
.
lld:C0033860
a
ncit:C7057
.
dgn-gda:DGNade1dad6c4096a1dfbac4785d8267f47
sio:SIO_000628
miriam-gene:27102
,
lld:C0033860
;
a
sio:SIO_001121
.
}
dgn-np:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_provenance
{
dgn-np:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_assertion
dcterms:description
"[Combinatorial analysis of exonic variations in the known genes of the candidate interval revealed that HCG27, PSORS1C3, OTF3, TCF19, HCR, STG, and HCG22 bore no alleles unique to risk haplotypes among the 10 sequenced haplotypes.]. 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:16642438
;
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:NP601590.RA-OYPxvo9EuFu9jOGP5gzrZ-gVSofB44c-4THdOI5vUs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}