@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo
> .
@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:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_head
{
this:
np:hasAssertion
dgn-np:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_assertion
;
np:hasProvenance
dgn-np:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_provenance
;
np:hasPublicationInfo
dgn-np:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_assertion
a
np:Assertion
.
dgn-np:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_provenance
a
np:Provenance
.
dgn-np:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0007789
a
ncit:C7057
.
dgn-gda:DGNb33bb0e4c1e947726785b32e8b81ce1a
sio:SIO_000628
miriam-gene:4397
,
lld:C0007789
;
a
sio:SIO_001121
.
}
dgn-np:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_provenance
{
dgn-np:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_assertion
dcterms:description
"[Second, increased familial risks were shown for disease subtypes for which susceptibility genes or familial clustering have not been demonstrated previously, including multiple sclerosis, sleep apnea, nerve, nerve root and plexus disorders, and cerebral palsy.]. 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:16899166
;
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:NP842377.RAc45MGzflVkl7JsAe_n-otB4U8CTtSzFSWIej5l6OMqo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:35+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" .
}