@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg
> .
@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:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_head
{
this:
np:hasAssertion
dgn-np:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_assertion
;
np:hasProvenance
dgn-np:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_provenance
;
np:hasPublicationInfo
dgn-np:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_assertion
a
np:Assertion
.
dgn-np:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_provenance
a
np:Provenance
.
dgn-np:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_assertion
{
miriam-gene:23414
a
ncit:C16612
.
lld:C0235833
a
ncit:C7057
.
dgn-gda:DGNc738d3f755661d02a63c7578208d9f9d
sio:SIO_000628
miriam-gene:23414
,
lld:C0235833
;
a
sio:SIO_001121
.
}
dgn-np:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_provenance
{
dgn-np:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_assertion
dcterms:description
"[Although our study identified sequence variants in FOG2 and PDGFRalpha, we have not definitively established the variants as mutations and we found no evidence that CDH commonly results from mutations in these genes.]. 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:17568391
;
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:NP278192.RA92htx9AnT8iMHUoOUX3vVxOuXfYngOKJ2nXDiIKgSkg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}