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- source_evidence_literature type ECO_0000212 NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_provenance.
- NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_assertion description "[Mosaicism for HOXA13 polyalanine expansions may be associated with a normal phenotype, making examination of parental DNA essential in apparently de novo HFGS cases to predict accurate recurrence risks.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_provenance.
- NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_assertion evidence source_evidence_literature NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_provenance.
- NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_assertion SIO_000772 23532960 NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_provenance.
- NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_assertion wasDerivedFrom befree-2016 NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_provenance.
- NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_assertion wasGeneratedBy ECO_0000203 NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1063935.RAS5HeFUttNdFAcN1_W-1fcRYNo6_NCWHkD6qL2AwFNnQ130_provenance.