Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance.
- NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_assertion description "[Thus, genetic and functional studies support the conclusion that heterozygous loss-of-function mutations in MYLK are associated with aortic dissections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance.
- NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_assertion evidence source_evidence_literature NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance.
- NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_assertion SIO_000772 21055718 NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance.
- NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_assertion wasDerivedFrom befree-20140225 NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance.
- NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_assertion wasGeneratedBy ECO_0000203 NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP643339.RAsEfB37R06yMdzgXvtCXMez14kW5XIjQB2KRyIwvqBFE130_provenance.