@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw
> .
@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:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_head
{
this:
np:hasAssertion
dgn-np:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_assertion
;
np:hasProvenance
dgn-np:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_provenance
;
np:hasPublicationInfo
dgn-np:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_assertion
a
np:Assertion
.
dgn-np:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_provenance
a
np:Provenance
.
dgn-np:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_assertion
{
miriam-gene:268
a
ncit:C16612
.
lld:C0238395
a
ncit:C7057
.
dgn-gda:DGN935c3b95cf1a48088678abb48e499b13
sio:SIO_000628
miriam-gene:268
,
lld:C0238395
;
a
sio:SIO_001121
.
}
dgn-np:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_provenance
{
dgn-np:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_assertion
dcterms:description
"[A rare form of familial male pseudohermaphroditism, the persistent Müllerian duct syndrome (PMDS) is characterized by persistence of uterus and Fallopian tubes in 46,XY phenotypic males and is ascribed to defects in the synthesis or action of anti-Müllerian hormone (AMH).]. 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:8162013
;
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:NP736658.RAwRY8TSiQWsPby4Rn9ux_VCasLLwho_Is_MqAJx7KSNw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:27+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" .
}