Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- befree-2016 importedOn "2016-02-19" NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion wasGeneratedBy ECO_0000203 NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion wasDerivedFrom befree-2016 NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion SIO_000772 9694901 NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion evidence source_evidence_literature NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.
- NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_assertion description "[We have previously reported two sisters with chronic Sandhoff disease who were heterozygous for the common HEXB deletion allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1401268.RAq-JOUqs7xLsLZyWPvxbgsuNyzkkFDxd6G8aFx02w7ag130_provenance.