Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance.
- NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_assertion description "[Homozygosity mapping was performed in five patients from a consanguineous family who presented with infantile mitochondrial encephalomyopathy attributed to isolated NADH:ubiquinone oxidoreductase (complex I) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance.
- NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_assertion evidence source_evidence_literature NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance.
- NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_assertion SIO_000772 18179882 NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance.
- NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_assertion wasDerivedFrom befree-20140225 NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance.
- NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_assertion wasGeneratedBy ECO_0000203 NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP307017.RASr-mZYloySLVGd24Sbzi6PAklbBX7smyP44yYvofE_k130_provenance.