@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ130_assertion
a
np:Assertion
.
dgn-np:NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ130_provenance
a
np:Provenance
.
dgn-np:NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ130_assertion
{
miriam-gene:5021
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGN795b92480bdc48e8107afaf5f1022649
sio:SIO_000628
miriam-gene:5021
,
lld:C1510586
;
a
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.
}
dgn-np:NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ130_provenance
{
dgn-np:NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ130_assertion
dcterms:description
"[The resulting pattern of findings, in general, confirmed the hypotheses of the significance of the genes involved in the development of affiliative behaviors in the manifestation of ASD (p values ranging from .000005 to .05); statistically speaking, the strongest results were obtained for allelic associations with the PRL, PRLR, and OXTR genes.]. 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:18207134
;
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:NP571169.RAB63tcs4KiNYbt85O0krq5mvMRaXDS0dgrfMI1E0MPnQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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
> , <
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> , <
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
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}