@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E
> .
@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/v3.0.0/void/
> .
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_head
{
this:
np:hasAssertion
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_assertion
;
np:hasProvenance
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_provenance
;
np:hasPublicationInfo
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_assertion
a
np:Assertion
.
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_provenance
a
np:Provenance
.
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_assertion
{
miriam-gene:3973
a
ncit:C16612
.
lld:C0013537
a
ncit:C7057
.
dgn-gda:DGNc150c1e2928b48fdbc1c4e3c82351977
sio:SIO_000628
miriam-gene:3973
,
lld:C0013537
;
a
sio:SIO_001121
.
}
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_provenance
{
dgn-np:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_assertion
dcterms:description
"[Together, these analyses suggest that exon 11 of human LHCGR could be more susceptible to mutation than the other 10 exons together and that activation of LHCGR, contingent to the somatic silencing of neighbouring ALF, could be linked to male-limited precocious puberty and pre-eclampsia.]. 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:16087288
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP536223.RAdvbEiDWcsWWaJkYAXWhLa1UEZX-eHy8BqlMpFzxn_7E130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:57+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}