@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o
> .
@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:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_head
{
this:
np:hasAssertion
dgn-np:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_assertion
;
np:hasProvenance
dgn-np:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_provenance
;
np:hasPublicationInfo
dgn-np:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_assertion
a
np:Assertion
.
dgn-np:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_provenance
a
np:Provenance
.
dgn-np:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_assertion
{
miriam-gene:4282
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGN1d2cbff0cd4a3b3b4b7302d22a8eb8db
sio:SIO_000628
miriam-gene:4282
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_provenance
{
dgn-np:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_assertion
dcterms:description
"[Additional research is warranted on the precise relationship between MIF and the behavioral components of autism spectrum disorder, the mechanism by which MIF contributes to autism spectrum disorder pathogenesis, and the clinical use of MIF genotyping.]. 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:18676531
;
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:NP216963.RAiIrQRdO2RTnsLmHTMuQf-EgkVLV-4whtdY2ecwXuI7o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}