@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:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_head { this: np:hasAssertion dgn-np:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_assertion; np:hasProvenance dgn-np:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_provenance; np:hasPublicationInfo dgn-np:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_publicationInfo; a np:Nanopublication . dgn-np:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_assertion a np:Assertion . dgn-np:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_provenance a np:Provenance . dgn-np:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_publicationInfo a np:PublicationInfo . } dgn-np:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_assertion { miriam-gene:5626 a ncit:C16612 . lld:C0271801 a ncit:C7057 . dgn-gda:DGN362181c1841999b48149d031b955dd0d sio:SIO_000628 miriam-gene:5626, lld:C0271801; a sio:SIO_001121 . } dgn-np:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_provenance { dgn-np:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_assertion dcterms:description "[The following topics are addressed: molecular mutations causing central hypothyroidism (isolated autosomal recessive TRH deficiency; autosomal recessive TRH-receptor inactivating mutations; TSH beta-subunit bio-inactivating mutations; Pit-1 mutations; Prop1 mutations; high molecular weight bio-inactive TSH); defects in response to TSH (mutations in the TSH receptor: TSH receptor gain-of-function mutations; TSH receptor loss-of-function mutations); defects in thyroid gland formation: transcription factor mutations (TTF-2 and Pax8); defects in peripheral thyroid hormone metabolism (defective intrapituitary conversion of T4 to T3; hemangioma consumption of thyroid hormone); and defects in tissue response to thyroid hormone (generalized thyroid hormone resistance, selective pituitary thyroid hormone resistance).]. 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:11508826; 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:NP365146.RAKySk5BfAZdd28IS55q8JfF2RhiX24LCTeSlseLDoJos130_publicationInfo { this: dcterms:created "2014-10-02T12:35:33+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }