@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_head
{
this:
np:hasAssertion
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_assertion
;
np:hasProvenance
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_assertion
a
np:Assertion
.
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_provenance
a
np:Provenance
.
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_assertion
{
miriam-gene:3973
a
ncit:C16612
.
lld:C0342549
a
ncit:C7057
.
dgn-gda:DGNcab56e5505df22733c38e1e456d77000
sio:SIO_000628
miriam-gene:3973
,
lld:C0342549
;
a
sio:SIO_001122
.
}
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_provenance
{
dgn-np:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_assertion
dcterms:description
"[To generate a mouse model for the human disease, we have introduced an aspartic acid to glycine mutation in amino acid residue 582 (D582G) of the mouse LHR gene corresponding to the most common D578G mutation found in boys with familial male-limited precocious puberty (FMPP).]. 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:23861372
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1094411.RAYPAewYl8yAuNAiyg8NsP8OYoZPuEsuYfaVBOYi5wCIg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:02+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}