Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.
- NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.
- NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_assertion evidence source_evidence_literature NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.
- NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_assertion SIO_000772 12970307 NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.
- NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_assertion wasDerivedFrom befree-20140225 NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.
- NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_assertion wasGeneratedBy ECO_0000203 NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.