Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance.
- NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_assertion description "[Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance.
- NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_assertion evidence source_evidence_literature NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance.
- NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_assertion SIO_000772 19400538 NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance.
- NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_assertion wasDerivedFrom befree-2016 NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance.
- NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_assertion wasGeneratedBy ECO_0000203 NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP735232.RARP1Pbj4hvzayYdX7CobsG7-T4HV2aAzQeXCk_ALvCYQ130_provenance.