Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion description "[De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion evidence source_evidence_literature NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion SIO_000772 21706002 NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion wasDerivedFrom befree-20140225 NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_assertion wasGeneratedBy ECO_0000203 NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722057.RALdPxI801_UmsSVWwiaV1YHBBW44CGo_Wtmtz1BuYrqU130_provenance.