@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU
> .
@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:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_head
{
this:
np:hasAssertion
dgn-np:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_assertion
;
np:hasProvenance
dgn-np:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_provenance
;
np:hasPublicationInfo
dgn-np:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_assertion
a
np:Assertion
.
dgn-np:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_provenance
a
np:Provenance
.
dgn-np:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_assertion
{
miriam-gene:2778
a
ncit:C16612
.
lld:C2931404
a
ncit:C7057
.
dgn-gda:DGNca43687587187cc6a96a85d27aaf5971
sio:SIO_000628
miriam-gene:2778
,
lld:C2931404
;
a
sio:SIO_001121
.
}
dgn-np:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_provenance
{
dgn-np:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_assertion
dcterms:description
"[The molecular overlap among these disorders indicates the need for different classification models and seriously alters our understanding of the mechanisms through which GNAS defects, together with the new recently described defects involving other components of the cAMP signalling cascade, cause AHO-related disorders.]. 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:25910998
;
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:NP1280475.RA11irgK6TOn68HFtSlTb4LiUQ_0JAO8aZz5EllOJ8DxU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:26+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" .
}