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- source_evidence_literature type ECO_0000212 NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_provenance.
- NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_assertion description "[Homozygous disruption of PCP genes in mice results in a spectrum of NTDs, including defects that affect the entire neural axis (craniorachischisis), cranial NTDs (exencephaly) and spina bifida.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_provenance.
- NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_assertion evidence source_evidence_literature NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_provenance.
- NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_assertion SIO_000772 21840926 NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_provenance.
- NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_assertion wasDerivedFrom befree-2016 NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_provenance.
- NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_assertion wasGeneratedBy ECO_0000203 NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP917024.RAghHmaLlAuFCTQDw87mr8qrORtoleuQClF4GsgXHsj7Y130_provenance.