Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance.
- NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_assertion description "[It is important for genetic counseling to be aware that their male offspring may not only be carriers of CFNS but may also be affected by mental retardation and anhidrotic ectodermal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance.
- NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_assertion evidence source_evidence_literature NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance.
- NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_assertion SIO_000772 17941886 NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance.
- NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_assertion wasDerivedFrom befree-20150227 NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance.
- NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_assertion wasGeneratedBy ECO_0000203 NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance.
- befree-20150227 importedOn "2015-02-27" NP366854.RAkgiXPtlvpzWwfwDlhsWF_eyd8uUHIC_lpFv4PJfp5Ys130_provenance.