@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_head { this: np:hasAssertion dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_assertion; np:hasProvenance dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_provenance; np:hasPublicationInfo dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_publicationInfo; a np:Nanopublication . dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_assertion a np:Assertion . dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_provenance a np:Provenance . dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_publicationInfo a np:PublicationInfo . } dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_assertion { miriam-gene:93986 a ncit:C16612 . lld:C0349231 a ncit:C7057 . dgn-gda:DGN033b8ac71a63688e545d8d61ded9406a sio:SIO_000628 miriam-gene:93986, lld:C0349231; a sio:SIO_001121 . } dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_provenance { dgn-np:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_assertion dcterms:description "[Speculations based on studies of the human abnormal-spindle-like, microcephaly-associated (ASPM) gene, the microcephaly primary autosomal recessive (MCPH) gene, and the forkhead box p2 (FOXP2) gene are made and incorporated into what is termed 'The pre-FOXP2 Hypothesis of Blood-Injection-Injury Phobia.' Finally, the author argues for a non-reductionistic fusion of 'distal (evolutionary) neurobiology' with clinical 'proximal neurobiology,' utilizing neurological heuristics.]. 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:16563589; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP962573.RAfNzElwPyfkKu9H8GBJai3JUiyREOtjjzG050NFpYitw130_publicationInfo { this: dcterms:created "2015-08-25T14:47:28+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }