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- source_evidence_literature type ECO_0000212 NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_provenance.
- NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_assertion description "[MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_provenance.
- NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_assertion evidence source_evidence_literature NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_provenance.
- NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_assertion SIO_000772 17427193 NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_provenance.
- NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_assertion wasDerivedFrom befree-20150227 NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_provenance.
- NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_assertion wasGeneratedBy ECO_0000203 NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP791398.RATbd_nr_tf1rEXwlnQClm_gto03FwNfSWF_DeA6EXuZM130_provenance.