Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance.
- NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_assertion description "[On analyzing CNTNAP2 polymorphisms in children with typical specific language impairment, we detected significant quantitative associations with nonsense-word repetition, a heritable behavioral marker of this disorder (peak association, P=5.0x10(-5) at SNP rs17236239).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance.
- NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_assertion evidence source_evidence_literature NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance.
- NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_assertion SIO_000772 18987363 NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance.
- NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_assertion wasDerivedFrom befree-20140225 NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance.
- NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_assertion wasGeneratedBy ECO_0000203 NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP648444.RAmvlyCna7R3hXEMUS_f0iDDmgQcoA-rQshOSifmOkQqw130_provenance.