Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance.
- NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_assertion description "[Four of nine informative fetal rhabdomyomas and embryonal rhabdomyosarcomas showed loss of heterozygosity (LOH) in the PTCH region with two of these (one fetal rhabdomyoma and one embryonal rhabdomyosarcoma) also showing LOH in the SUFU region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance.
- NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_assertion evidence source_evidence_literature NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance.
- NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_assertion SIO_000772 16294371 NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance.
- NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_assertion wasDerivedFrom befree-2016 NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance.
- NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_assertion wasGeneratedBy ECO_0000203 NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP523131.RAK0F_HDXY2cJRntzGP58cToiE5ft4xQefNT9SNgLRVZQ130_provenance.