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- source_evidence_literature type ECO_0000212 NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_provenance.
- NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_assertion description "[We therefore determine in this study the relative frequency of mutations in PLCE1, WT1 or LAMB2 as the cause of IDMS in a worldwide cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_provenance.
- NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_assertion evidence source_evidence_literature NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_provenance.
- NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_assertion SIO_000772 18065803 NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_provenance.
- NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_assertion wasDerivedFrom befree-2016 NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_provenance.
- NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_assertion wasGeneratedBy ECO_0000203 NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_provenance.
- befree-2016 importedOn "2016-02-19" NP644172.RAwLhQ2nbg_8TxPEb5Qex9tL69sOYS1NBl1DcieP_DOA4130_provenance.