@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI
> .
@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:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_head
{
this:
np:hasAssertion
dgn-np:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_assertion
;
np:hasProvenance
dgn-np:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_provenance
;
np:hasPublicationInfo
dgn-np:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_assertion
a
np:Assertion
.
dgn-np:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_provenance
a
np:Provenance
.
dgn-np:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_assertion
{
miriam-gene:395
a
ncit:C16612
.
lld:C0796070
a
ncit:C7057
.
dgn-gda:DGNcc7c1343c1229e2f8f576b34dc644e21
sio:SIO_000628
miriam-gene:395
,
lld:C0796070
;
a
sio:SIO_001121
.
}
dgn-np:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_provenance
{
dgn-np:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_assertion
dcterms:description
"[Future molecular studies in karyotypically normal female MLS patients to detect submicroscopic rearrangements including the ARHGAP6 gene as well as mutation screening of ARHGAP6 in patients with no obvious chromosomal rearrangements will clarify the role of this gene in MLS syndrome.]. 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:12900578
;
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:NP159396.RAy7zmpcIXqOKYEuIsHckEQtWb2pVqihvS1ae5izOl5tI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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: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" .
}