Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- befree-2016 importedOn "2016-02-19" NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion wasGeneratedBy ECO_0000203 NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion wasDerivedFrom befree-2016 NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion SIO_000772 22344793 NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion evidence source_evidence_literature NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion description "[Association of X-linked hydrocephalus and Hirschsprung disease: report of a new patient with a mutation in the L1CAM gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.