Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance.
- NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_assertion description "[This report emphasizes concurrently that ABCC6 may be a relevant candidate gene in some cases of GACI with no mutations in the ENPP1 gene, and that GACI may be an atypical and severe end of the vascular phenotype spectrum of PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance.
- NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_assertion evidence source_evidence_literature NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance.
- NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_assertion SIO_000772 20034067 NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance.
- NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_assertion wasDerivedFrom befree-20140225 NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance.
- NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_assertion wasGeneratedBy ECO_0000203 NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP222904.RAH9uPlruoYl09F_82ehdzkpF7NTe8XE-yyaRLUuH_jX0130_provenance.