Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance.
- NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_assertion description "[Acute encephalopathy with a truncation mutation in the SCN1A gene: a case report.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance.
- NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_assertion evidence source_evidence_literature NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance.
- NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_assertion SIO_000772 20491869 NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance.
- NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_assertion wasDerivedFrom befree-2016 NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance.
- NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_assertion wasGeneratedBy ECO_0000203 NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP813803.RAuwGaF_mSXpFC26vg3Tng08Kya7oVoCH-OH22dSt07HQ130_provenance.