@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA
> .
@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:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_head
{
this:
np:hasAssertion
dgn-np:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_assertion
;
np:hasProvenance
dgn-np:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_provenance
;
np:hasPublicationInfo
dgn-np:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_assertion
a
np:Assertion
.
dgn-np:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_provenance
a
np:Provenance
.
dgn-np:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_assertion
{
miriam-gene:558
a
ncit:C16612
.
lld:C0162809
a
ncit:C7057
.
dgn-gda:DGNb037c2491b2a31820b67f7d268992a3f
sio:SIO_000628
miriam-gene:558
,
lld:C0162809
;
a
sio:SIO_001121
.
}
dgn-np:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_provenance
{
dgn-np:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_assertion
dcterms:description
"[The objective of the study was to test whether the absence of Axl would alter reproductive function in mice and that mutations in AXL are present in patients with Kallmann syndrome (KS) or normosmic idiopathic hypogonadotropic hypogonadism (nIHH).]. 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:24476074
;
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:NP1150075.RACAFJQuhaWMkTrsOxwOf9KeUiHjagTm0hvSrH9sX6noA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:27+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" .
}