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- source_evidence_literature type ECO_0000212 NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion description "[Mutations in ROR2 have been shown to cause two distinct human disorders, autosomal recessive Robinow syndrome and dominantly inherited Brachydactyly type B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion evidence source_evidence_literature NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion SIO_000772 17665217 NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion wasDerivedFrom befree-20140225 NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_assertion wasGeneratedBy ECO_0000203 NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP665513.RACx2bTHGhLxKopCuV_3PcfFioMp1INTOMnMNUj8spljI130_provenance.