@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc
> .
@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:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_head
{
this:
np:hasAssertion
dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_assertion
;
np:hasProvenance
dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_provenance
;
np:hasPublicationInfo
dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_assertion
a
np:Assertion
.
dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_provenance
a
np:Provenance
.
dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_assertion
{
miriam-gene:3730
a
ncit:C16612
.
lld:C0162809
a
ncit:C7057
.
dgn-gda:DGN40faaff324772b21081370ad15bdab4a
sio:SIO_000628
miriam-gene:3730
,
lld:C0162809
;
a
sio:SIO_001121
.
}
dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_provenance
{
dgn-np:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_assertion
dcterms:description
"[Sequence variations may be pseudogene products rather than true polymorphisms, so we should always determine if the position where the variation is located differs between KAL1 and its pseudogene, because it has been suggested that the presence of various polymorphisms in affected individuals could be the cause of KS.]. 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:15636431
;
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:NP475222.RA_p3dg6s9ikWhrDsXTXmIJw49kUTnUeG_aRpiS0wNvzc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:20+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" .
}