Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance.
- NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_assertion description "[Microcephalin (MCPH1) is a gene mutated in primary microcephaly, an autosomal recessive neurodevelopmental disorder in which there is a marked reduction in brain size.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance.
- NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_assertion evidence source_evidence_literature NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance.
- NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_assertion SIO_000772 15199523 NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance.
- NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_assertion wasDerivedFrom befree-2016 NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance.
- NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_assertion wasGeneratedBy ECO_0000203 NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance.
- befree-2016 importedOn "2016-02-19" NP448347.RAgPa2B7uFac3EIyGsCZzsxm-VE_XEVx2uFZvKf4ubWrg130_provenance.