Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance.
- NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_assertion wasGeneratedBy ECO_0000203 NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance.
- NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_assertion wasDerivedFrom befree-20150227 NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance.
- NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_assertion SIO_000772 22310223 NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance.
- NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_assertion evidence source_evidence_literature NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance.
- NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_assertion description "[Clinical molecular diagnostic centers routinely screen SHH, ZIC2, SIX3 and TGIF for mutations that can help to explain holoprosencephaly and related brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP504580.RAqdgs99Hbi1KokgQcgU_Jnbd83dU37vejI_o9tw6WiZ8130_provenance.