@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg
> .
@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:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_head
{
this:
np:hasAssertion
dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_assertion
;
np:hasProvenance
dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_provenance
;
np:hasPublicationInfo
dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_assertion
a
np:Assertion
.
dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_provenance
a
np:Provenance
.
dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_assertion
{
miriam-gene:64220
a
ncit:C16612
.
lld:C0265783
a
ncit:C7057
.
dgn-gda:DGN8c8b7aec51ce3d2565cca268c72039d5
sio:SIO_000628
miriam-gene:64220
,
lld:C0265783
;
a
sio:SIO_001121
.
}
dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_provenance
{
dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_assertion
dcterms:description
"[Five other fetuses presenting at least one of the two major signs of clinical anophthalmia or pulmonary hypoplasia with at least one of the two associated signs of diaphragmatic closure defect or cardiopathy had no STRA6 mutations.]. 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:17503335
;
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:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}