@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM
> .
@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:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_head
{
this:
np:hasAssertion
dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_assertion
;
np:hasProvenance
dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_provenance
;
np:hasPublicationInfo
dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_assertion
a
np:Assertion
.
dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_provenance
a
np:Provenance
.
dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_assertion
{
miriam-gene:55349
a
ncit:C16612
.
lld:C0152021
a
ncit:C7057
.
dgn-gda:DGNbd8117d66eae9aeb17681d341247631a
sio:SIO_000628
miriam-gene:55349
,
lld:C0152021
;
a
sio:SIO_001121
.
}
dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_provenance
{
dgn-np:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_assertion
dcterms:description
"[In the candidate region 12q13 of simple congenital heart disease(CHD), four single nucleotide polymorphisms(SNPs) in HOXC4 gene were chosen in order to investigate the distribution of SNP and haplotypes in simple CHD patients and normal people.]. 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:16215934
;
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:NP245865.RAPcPBWiTY03UtHZ603i2aVGWICvAKsZYnQeNFXPKp6IM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}