Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance.
- NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_assertion description "[We present a male child with a de novo dup(17)(p11.2p11.2) and he does not possess any autistic features, but is characterized by severe speech and language impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance.
- NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_assertion evidence source_evidence_literature NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance.
- NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_assertion SIO_000772 22178197 NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance.
- NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_assertion wasDerivedFrom befree-20140225 NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance.
- NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_assertion wasGeneratedBy ECO_0000203 NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP197918.RALY_qoWOnUFNDKsSjW_0e3gj7DH8CvoIO0xr62txdxC8130_provenance.