Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance.
- NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_assertion description "[Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance.
- NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_assertion evidence source_evidence_literature NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance.
- NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_assertion SIO_000772 23791568 NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance.
- NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_assertion wasDerivedFrom befree-20150227 NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance.
- NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_assertion wasGeneratedBy ECO_0000203 NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP556451.RAQoejU0XcPI5v2cZT7OEKp-cIaIiLT_2M0wV1JAQyYAI130_provenance.