@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I
> .
@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:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_head
{
this:
np:hasAssertion
dgn-np:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_assertion
;
np:hasProvenance
dgn-np:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_provenance
;
np:hasPublicationInfo
dgn-np:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_assertion
a
np:Assertion
.
dgn-np:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_provenance
a
np:Provenance
.
dgn-np:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_assertion
{
miriam-gene:6910
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGNeeb80d46669866f2ad72c3161b2e34dd
sio:SIO_000628
miriam-gene:6910
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_provenance
{
dgn-np:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_assertion
dcterms:description
"[As part of a larger study, high density, single nucleotide polymorphism (SNP) scanning was used to explore the relationship between TBX5 gene polymorphism and susceptibility to ventricular septal defect not associated with forelimb malformation in the Chinese Han population.]. 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:19187613
;
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:NP455907.RAZKpkrbwgEAKuSSHAV3gX_5msoIuwVeyZYOEYyvxB-7I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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" .
}