@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY
> .
@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:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_head
{
this:
np:hasAssertion
dgn-np:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_assertion
;
np:hasProvenance
dgn-np:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_provenance
;
np:hasPublicationInfo
dgn-np:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_assertion
a
np:Assertion
.
dgn-np:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_provenance
a
np:Provenance
.
dgn-np:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_assertion
{
miriam-gene:6736
a
ncit:C16612
.
lld:C0950122
a
ncit:C7057
.
dgn-gda:DGN7943c66f8feadd461abcb8f761172cbe
sio:SIO_000628
miriam-gene:6736
,
lld:C0950122
;
a
sio:SIO_001121
.
}
dgn-np:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_provenance
{
dgn-np:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_assertion
dcterms:description
"[These data suggest that in the Frasier syndrome, XY sex reversal and renal failure could be the result of either faulty gene(s) located downstream in the sex differentiation pathway during embryogenesis, or impaired SRY regulation.]. 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:1478624
;
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:NP414721.RAHhGcUhvSANWSDfWHKNFoIHzocqQVjIzU_I8e1vbYBgY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:06+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" .
}