Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance.
- NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_assertion description "[We hypothesized that neural pathways downstream of FOXP2 influence more common phenotypes, such as specific language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance.
- NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_assertion evidence source_evidence_literature NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance.
- NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_assertion SIO_000772 18987363 NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance.
- NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_assertion wasDerivedFrom befree-20150227 NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance.
- NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_assertion wasGeneratedBy ECO_0000203 NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP962582.RASR-szU1qy7CcDG9VHfUeUAith7hDx_-VfBZCRQ3JNkY130_provenance.