Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance.
- NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_assertion description "[Huntington disease (HD) is an inherited neurological disorder caused by a polyglutamine expansion in the protein huntingtin and is characterized by selective neurodegeneration that preferentially occurs in striatal medium spiny neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance.
- NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_assertion evidence source_evidence_literature NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance.
- NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_assertion SIO_000772 20018729 NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance.
- NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_assertion wasDerivedFrom befree-20150227 NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance.
- NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_assertion wasGeneratedBy ECO_0000203 NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP445354.RAEQ7p2IH2Af7_sHpNrHOhS6Gjj5s4TB2N5xN75hNIHlo130_provenance.