@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4
> .
@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:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_head
{
this:
np:hasAssertion
dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_assertion
;
np:hasProvenance
dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_provenance
;
np:hasPublicationInfo
dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_assertion
a
np:Assertion
.
dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_provenance
a
np:Provenance
.
dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_assertion
{
miriam-gene:60675
a
ncit:C16612
.
lld:C0162809
a
ncit:C7057
.
dgn-gda:DGN183eafa83b8f681e641c5b9d2cfbb854
sio:SIO_000628
miriam-gene:60675
,
lld:C0162809
;
a
sio:SIO_001121
.
}
dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_provenance
{
dgn-np:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_assertion
dcterms:description
"[Some cases of mutations of FGFR1, and more rarely of its ligand FGF8, or of PROKR2 or its ligand PROK2 have been shown in women suffering from Kallmann syndrome or its hyposmic or normosmic variant.]. 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:20363464
;
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:NP803940.RAPodXhUIzCA3PL4Lw9wHNxrltrCg0eOrFE0qPJ92wmU4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:49+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" .
}