@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY
> .
@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:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_head
{
this:
np:hasAssertion
dgn-np:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_assertion
;
np:hasProvenance
dgn-np:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_provenance
;
np:hasPublicationInfo
dgn-np:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_assertion
a
np:Assertion
.
dgn-np:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_provenance
a
np:Provenance
.
dgn-np:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_assertion
{
miriam-gene:3977
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN66f2b4278f4715285d75ae5518f7b81c
sio:SIO_000628
miriam-gene:3977
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_provenance
{
dgn-np:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_assertion
dcterms:description
"[In control fertile women, simultaneous intense apical staining of LIFR and gp130 together with faint SOCS1 staining was observed in epithelial cells, whereas the opposite was seen in most women with unexplained infertility.]. 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:18684446
;
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:NP242995.RA2RJu4WlIjKVnKfRBWJYyOdz9EFdEyv2XSbI0tvJlNpY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}