@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0
> .
@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:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_head
{
this:
np:hasAssertion
dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_assertion
;
np:hasProvenance
dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_provenance
;
np:hasPublicationInfo
dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_assertion
a
np:Assertion
.
dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_provenance
a
np:Provenance
.
dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_assertion
{
miriam-gene:2296
a
ncit:C16612
.
lld:C0018817
a
ncit:C7057
.
dgn-gda:DGN5e0f2299eab808a9007bd834b8f8cb43
sio:SIO_000628
miriam-gene:2296
,
lld:C0018817
;
a
sio:SIO_001121
.
}
dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_provenance
{
dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_assertion
dcterms:description
"[This is further supported by our studies showing that mutations in the FKHL7 gene were associated with defects in the anterior segment of the eye as well as atrial septal defects or mitral valve defects.]. 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:10474162
;
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:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}