@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_head
{
this:
np:hasAssertion
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_assertion
;
np:hasProvenance
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_provenance
;
np:hasPublicationInfo
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_assertion
a
np:Assertion
.
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_provenance
a
np:Provenance
.
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_assertion
{
miriam-gene:4016
a
ncit:C16612
.
lld:C0206368
a
ncit:C7057
.
dgn-gda:DGN9147f38f4869455bfe79e383f3b38591
sio:SIO_000628
miriam-gene:4016
,
lld:C0206368
;
a
sio:SIO_001121
.
}
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_provenance
{
dgn-np:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_assertion
dcterms:description
"[Recent human genetic association studies have identified changes occurring in the LOXL1 gene as an important risk factor for XFS but also indicated that other factors contributing to risk likely exist.]. 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:19029039
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP705335.RAOpNyoBBpRBS2xZ2SgFWLfplQWujCXW3U4d3N461mNIo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:04+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}