Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance.
- NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_assertion description "[Holoprosencephaly (HPE), a common human congenital anomaly defined by a failure to delineate the midline of the forebrain and/or midface, is associated with diminished Sonic hedgehog (SHH)-pathway activity in development of these structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance.
- NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_assertion evidence source_evidence_literature NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance.
- NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_assertion SIO_000772 21802063 NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance.
- NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_assertion wasDerivedFrom befree-2016 NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance.
- NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_assertion wasGeneratedBy ECO_0000203 NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance.
- befree-2016 importedOn "2016-02-19" NP913499.RABmq1czB5ZcrHsJY-R9v_-biN7zpbGKE5rbctWIgrMjo130_provenance.