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- source_evidence_literature type ECO_0000212 NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_provenance.
- befree-20150227 importedOn "2015-02-27" NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_provenance.
- NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_assertion wasGeneratedBy ECO_0000203 NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_provenance.
- NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_assertion wasDerivedFrom befree-20150227 NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_provenance.
- NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_assertion SIO_000772 23144470 NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_provenance.
- NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_assertion evidence source_evidence_literature NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_provenance.
- NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_assertion description "[We investigated the underlying molecular mechanism of GNAS imprinting defects in two patients with sporadic PHP1b.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429930.RApqNeM-w4vlaPa9YMg39woYYsxA6cLp0Q6RriWIdcano130_provenance.