@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04
> .
@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:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_head
{
this:
np:hasAssertion
dgn-np:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_assertion
;
np:hasProvenance
dgn-np:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_provenance
;
np:hasPublicationInfo
dgn-np:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_assertion
a
np:Assertion
.
dgn-np:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_provenance
a
np:Provenance
.
dgn-np:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_assertion
{
miriam-gene:2316
a
ncit:C16612
.
lld:C2678104
a
ncit:C7057
.
dgn-gda:DGN3d38486b8e2fe923cdd9361153f2b944
sio:SIO_000628
miriam-gene:2316
,
lld:C2678104
;
a
sio:SIO_001121
.
}
dgn-np:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_provenance
{
dgn-np:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_assertion
dcterms:description
"[These results suggest that mutations in ARFGEF2 may impair targeted transport of FLNA to the cell surface within neural progenitors along the neuroependyma and that disruption of these cells could contribute to PH formation.]. 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:16320251
;
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:NP430095.RAXCTmNXciI2C2_xHbcRG4qS5J9e_2xFQ17zr_wRY8h04130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}