@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k
> .
@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:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_head
{
this:
np:hasAssertion
dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_assertion
;
np:hasProvenance
dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_provenance
;
np:hasPublicationInfo
dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_assertion
a
np:Assertion
.
dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_provenance
a
np:Provenance
.
dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_assertion
{
miriam-gene:2263
a
ncit:C16612
.
lld:C0001193
a
ncit:C7057
.
dgn-gda:DGNd679c59c0e5d25545d11c0e5815e0418
sio:SIO_000628
miriam-gene:2263
,
lld:C0001193
;
a
sio:SIO_001121
.
}
dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_provenance
{
dgn-np:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_assertion
dcterms:description
"[The objective of this study was to determine whether there were any differences in the prevalence of ophthalmic features in Apert syndrome when comparing the Ser252Trp and Pro253Arg mutations in FGFR2.]. 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:17251833
;
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:NP196796.RAX3P95hggLuvMke3Cbx7Pjhqz2D-gzOdpy8MQyRf8n6k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}