Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.
- NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.
- NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_assertion evidence source_evidence_literature NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.
- NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_assertion SIO_000772 11438991 NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.
- NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_assertion wasDerivedFrom befree-2016 NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.
- NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_assertion wasGeneratedBy ECO_0000203 NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.
- befree-2016 importedOn "2016-02-19" NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.