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- source_evidence_literature type ECO_0000212 NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance.
- NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_assertion description "[Common variants in contactin-associated protein-like 2 (CNTNAP2), a neurexin superfamily member, have been associated with several allied neurodevelopmental disorders, including autism and specific language impairment, and CNTNAP2 is highly expressed in frontal lobe circuits in the developing human brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance.
- NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_assertion evidence source_evidence_literature NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance.
- NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_assertion SIO_000772 21048216 NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance.
- NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_assertion wasDerivedFrom befree-20150227 NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance.
- NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_assertion wasGeneratedBy ECO_0000203 NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP881331.RAUKkeBKRrJK2OacAFhy4bh1F0h4TxpD90ewtLLjkUJdo130_provenance.