Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.
- NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_assertion description "[Autosomal recessive hypercholesterolaemia (ARH), characterized clinically by severe inherited hypercholesterolaemia, is caused by recessive null mutations in LDLRAP1 (formerly ARH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.
- NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_assertion evidence source_evidence_literature NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.
- NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_assertion SIO_000772 17761685 NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.
- NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_assertion wasDerivedFrom befree-20140225 NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.
- NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_assertion wasGeneratedBy ECO_0000203 NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.