@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw
> .
@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:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_head
{
this:
np:hasAssertion
dgn-np:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_assertion
;
np:hasProvenance
dgn-np:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_provenance
;
np:hasPublicationInfo
dgn-np:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_assertion
a
np:Assertion
.
dgn-np:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_provenance
a
np:Provenance
.
dgn-np:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0432475
a
ncit:C7057
.
dgn-gda:DGNe572b127686af9c2684d07ba74f609ce
sio:SIO_000628
miriam-gene:3342
,
lld:C0432475
;
a
sio:SIO_001121
.
}
dgn-np:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_provenance
{
dgn-np:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_assertion
dcterms:description
"[The two Xpter (XPAR1) pseudoautosomal regions present in this XX male suggest the need to reevaluate XX males using CGH and PCR to characterize the clinical variability in XX males due to genes other than those located on the Y chromosome.]. 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:12095512
;
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:NP922256.RAnqsOnuRD1xlLq2dQWj_jFWvtATWdhacKY_0nzBTkrUw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}