@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0> .
@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:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_head {
  this: np:hasAssertion dgn-np:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_assertion ;
    np:hasProvenance dgn-np:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_provenance ;
    np:hasPublicationInfo dgn-np:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_assertion a np:Assertion .
  dgn-np:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_provenance a np:Provenance .
  dgn-np:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_assertion {
  miriam-gene:4159 a ncit:C16612 .
  lld:C0028754 a ncit:C7057 .
  dgn-gda:DGNa076ba78df86bfda052d82129b11fede sio:SIO_000628 miriam-gene:4159 , lld:C0028754 ;
    a sio:SIO_001121 .
}
dgn-np:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_provenance {
  dgn-np:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_assertion dcterms:description "[While MC3R mutations are unlikely to result in an autosomal dominant form of monogenic obesity given the lack of strong co-segregation in family studies, the studies so far provided evidence that MC3R can be one of the genes which contributes to increased adiposity, and exert an effect on the human phenotype.]. 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:23280863 ;
    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:NP213974.RASMOqk0xKpMzHcP7m2H-PitfXMJmYj7vgQZGkhKPUMX0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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> ;
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}