Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance.
- NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_assertion description "[We identified five patients from four independent families displaying the IRIDA picture with truncating biallelic mutations in TMPRSS6, one of which is novel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance.
- NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_assertion evidence source_evidence_literature NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance.
- NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_assertion SIO_000772 23180434 NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance.
- NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_assertion wasDerivedFrom befree-20150227 NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance.
- NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_assertion wasGeneratedBy ECO_0000203 NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977546.RAFkWwqOf13WaDk22JVvDDfxdJe-UyTbjF3H6fVD7zv2U130_provenance.