Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.
- NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_assertion description "[Our data establish recessive mutations in CDH3 as the molecular cause of hypotrichosis with juvenile macular dystrophy and expand our understanding of the pathophysiology of this intriguing disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.
- NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_assertion evidence source_evidence_literature NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.
- NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_assertion SIO_000772 12445216 NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.
- NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_assertion wasDerivedFrom befree-2016 NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.
- NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_assertion wasGeneratedBy ECO_0000203 NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.
- befree-2016 importedOn "2016-02-19" NP375345.RAil4RJGSdxRs5H26H8FGxKOhYPkuP6xXrS6i7uSEr_08130_provenance.