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- source_evidence_literature type ECO_0000212 NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_provenance.
- NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_assertion description "[Employing Affymetrix SNP microarrays, 297 single nucleotide polymorphisms (SNPs) covering the GRM7 gene were selected and analyzed in ASD patients (n=22), non-ASD patients [n=14, including seven patients with development delay (DD)/mental retardation (MR), four patients with language delay (LD), and three patients with attention deficit hyperactivity disorder (ADHD)] and normal control subjects (n=18).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_provenance.
- NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_assertion evidence source_evidence_literature NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_provenance.
- NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_assertion SIO_000772 23201551 NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_provenance.
- NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_assertion wasDerivedFrom befree-20140225 NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_provenance.
- NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_assertion wasGeneratedBy ECO_0000203 NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697093.RA5_f4QaTYEl7XmrS3xkfTWzo-EKo5AhE_PbbgSd3cI8g130_provenance.