Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance.
- befree-2016 importedOn "2016-02-19" NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance.
- NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_assertion wasGeneratedBy ECO_0000203 NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance.
- NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_assertion wasDerivedFrom befree-2016 NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance.
- NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_assertion SIO_000772 20858596 NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance.
- NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_assertion evidence source_evidence_literature NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance.
- NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_assertion description "[Mutations in transcription factor FOXP2 cause difficulties mastering fluent speech (developmental verbal dyspraxia, DVD), whereas mutations of sushi-repeat protein SRPX2 lead to epilepsy of the rolandic (sylvian) speech areas, with DVD or with bilateral perisylvian polymicrogyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840822.RA48SIWD2kyVpkR8Iq5eqXYrO2Ms0bcOL-N6ryYzu1s88130_provenance.