@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM
> .
@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:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_head
{
this:
np:hasAssertion
dgn-np:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_assertion
;
np:hasProvenance
dgn-np:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_provenance
;
np:hasPublicationInfo
dgn-np:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_assertion
a
np:Assertion
.
dgn-np:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_provenance
a
np:Provenance
.
dgn-np:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_assertion
{
miriam-gene:2691
a
ncit:C16612
.
lld:C2940786
a
ncit:C7057
.
dgn-gda:DGN514a1ad5d57608fcba1a9c8e63cfdfc8
sio:SIO_000628
miriam-gene:2691
,
lld:C2940786
;
a
sio:SIO_001121
.
}
dgn-np:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_provenance
{
dgn-np:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_assertion
dcterms:description
"[Patients may have the classic Albright's hereditary osteodystrophy (AHO) phenotype and can develop resistance to thyroid stimulating hormone (TSH), gonadotropins, growth hormone releasing hormone (GHRH), and other hormones that rely on the Gsalpha protein to regulate signal transmission at their receptors.]. 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:16995592
;
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:NP544348.RAQwh4WTYMkIzgJbIoC1faMY5CaoK6pypocQOAsNQCnpM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:28+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" .
}