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- source_evidence_literature type ECO_0000212 NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_provenance.
- NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_assertion description "[This study supports the recently hypothesized involvement of the ABC7 gene in XLSA/A and highlights a protein structure region of importance to this syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_provenance.
- NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_assertion evidence source_evidence_literature NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_provenance.
- NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_assertion SIO_000772 11843825 NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_provenance.
- NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_assertion wasDerivedFrom befree-2016 NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_provenance.
- NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_assertion wasGeneratedBy ECO_0000203 NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP345058.RAhwUK6N2KepZJgLHoNP2vOC6XnJ0saNyzT_HOWgLV9JQ130_provenance.