@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE
> .
@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:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_head
{
this:
np:hasAssertion
dgn-np:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_assertion
;
np:hasProvenance
dgn-np:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_provenance
;
np:hasPublicationInfo
dgn-np:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_assertion
a
np:Assertion
.
dgn-np:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_provenance
a
np:Provenance
.
dgn-np:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_assertion
{
miriam-gene:5604
a
ncit:C16612
.
lld:C0028326
a
ncit:C7057
.
dgn-gda:DGN9d62223fab38399b7dc851ab3d150642
sio:SIO_000628
miriam-gene:5604
,
lld:C0028326
;
a
sio:SIO_001121
.
}
dgn-np:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_provenance
{
dgn-np:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_assertion
dcterms:description
"[Mutational analysis of the affected MEK1 and MEK2 exons did not reveal occurrence of mutations among 75 patients with Noonan syndrome, confirming the low prevalence of MEK gene defects in this disorder.]. 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:19156172
;
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:NP412551.RAeRA1Ilqe6aPQ7pfVvuANsxbnpi8a6sXflveMkSvZDmE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}